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Instilling Eye Drops

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1. Shortening of Interpupillary Distance after Instillation of Topical Prostaglandin Analogue Eye Drops. (PubMed)

Shortening of Interpupillary Distance after Instillation of Topical Prostaglandin Analogue Eye Drops. To investigate changes in the interpupillary distance (IPD) after continual instillation of topical prostaglandin analogues (PGAs) in glaucoma patients as an objective indicator of prostaglandin-associated periorbitopathy (PAP).Retrospective, comparative case series.SETTING: Institutional.Patients (n=152) with glaucoma. Inclusion criteria were visual acuities exceeding 10/20 bilaterally (...) and no intraocular surgery during observation.First-time bilateral instillation of bimatoprost, travoprost, latanoprost, or tafluprost and IPDs measured by automatic refractometry. IPDs, intraocular pressures (IOPs), and refractive errors were measured before and after continual drug administration (treatment, 2-24 months).Post-treatment changes in IPDs. Sixty-one untreated patients served as controls.The IPDs shortened significantly (P<0.001) post-treatment (-0.80±2.1 mm); the controls remained unchanged (0.05

2019 American Journal of Ophthalmology

2. Factors affecting eye drop instillation in glaucoma patients with visual field defect. (Full text)

Factors affecting eye drop instillation in glaucoma patients with visual field defect. To investigate the success rate of eye drop instillation in glaucoma patients with visual field defect as well as non-glaucoma volunteers. Factors that may affect the success rate of eye drop instillation were also evaluated.A prospective, observational study.Seventy-eight glaucoma patients and 85 non-glaucoma volunteers were recruited in this study.Open angle glaucoma patients with visual field defect (...) as well as non-glaucoma volunteers were asked to video record their procedures of eye drop instillation using a 5-mL plastic bottle of artificial tear solution. Success of eye drop instillation was judged on video based on the first one drop of solution successfully applied on the cornea, by two investigators.Success rate of eye drop instillation in glaucoma patients and non-glaucoma volunteers. Factors related to success rate of eye drop instillation, such as visual field defect and clinical

2017 PLoS ONE PubMed

3. Evaluating Eye Drop Instillation Technique and Its Determinants in Glaucoma Patients (Full text)

Evaluating Eye Drop Instillation Technique and Its Determinants in Glaucoma Patients To evaluate eye drop instillation technique and to explore its determinants in glaucoma patients.One hundred and thirteen patients diagnosed with glaucoma and self-administering topical antiglaucoma eye drops for at least 1 month were evaluated. All patients instilled artificial tear solution in one eye as they would do at home. The whole process was evaluated by two study staff. A comprehensive score system (...) associated with eye drop instillation techniques was used to quantify the instillation technique and explore its determinants such as demographic and clinical characteristics.Half of the patients (48.67%) finished the administration of eye drop on first attempt.1.7 eye drops were squeezed out on average. 43 patients (37.17%) got contact with ocular surface or adnexa. Only 19.7% patients had eye drop instillation techniques being defined as well. 11 patients (9.7%) had prior instruction regarding using

2018 Journal of ophthalmology PubMed

4. Efficacy and Necessity of Time Interval Between Instillation of Two Glaucoma Eye Drops

Efficacy and Necessity of Time Interval Between Instillation of Two Glaucoma Eye Drops Efficacy and Necessity of Time Interval Between Instillation of Two Glaucoma Eye Drops - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies (...) before adding more. Efficacy and Necessity of Time Interval Between Instillation of Two Glaucoma Eye Drops The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. of clinical studies and talk to your health care provider before participating. Read our for details. ClinicalTrials.gov Identifier: NCT03220490 Recruitment Status : Not yet recruiting First Posted

2017 Clinical Trials

5. A Study of the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of RO7058584 Following 7 Days of Instillation of Eye Drops in Patients With Primary Open Angle Glaucoma or Ocular Hypertension

A Study of the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of RO7058584 Following 7 Days of Instillation of Eye Drops in Patients With Primary Open Angle Glaucoma or Ocular Hypertension A Study of the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of RO7058584 Following 7 Days of Instillation of Eye Drops in Patients With Primary Open Angle Glaucoma or Ocular Hypertension - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer (...) to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding more. A Study of the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of RO7058584 Following 7 Days of Instillation of Eye Drops in Patients With Primary Open Angle Glaucoma or Ocular Hypertension The safety and scientific validity of this study

2017 Clinical Trials

6. Evaluation of Short Term Use of Experimental Eye Drops BHVI2, 0.02% Atropine and BHVI2 Plus 0.02% Atropine Eye Drops

Outcome Measures : Change in pupillary diameter [ Time Frame: At baseline, at two-week and one-month visits ] Measure and compare the photopic and mesopic pupil size (milimeters) before and after instillation of eye drops Change in accommodative amplitude [ Time Frame: At baseline, at two-week and one-month visits ] Measure and compare the accommodative amplitude (diopters) before and after instillation of eye drops Eligibility Criteria Go to Information from the National Library of Medicine Choosing (...) Evaluation of Short Term Use of Experimental Eye Drops BHVI2, 0.02% Atropine and BHVI2 Plus 0.02% Atropine Eye Drops Evaluation of Short Term Use of Experimental Eye Drops BHVI2, 0.02% Atropine and BHVI2 Plus 0.02% Atropine Eye Drops - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number

2018 Clinical Trials

7. Evaluation of a New Method for Instilling Eye Drops

Evaluation of a New Method for Instilling Eye Drops Evaluation of a New Method for Instilling Eye Drops - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding more. Evaluation of a New Method for Instilling Eye Drops (...) : The purpose of this project is to demonstrate that there is a new easier method to instill eye drops in ones own eye that is as effective as applying a drop directly to their open eye. The benefits of this new method include better medication compliance and reduced patient anxiety from instilling their eye drops. This secondary benefit should remove the "approach-avoidance response" that prompts some patients to delay or give-up on instilling their drops just to avoid the angst and frustration produced

2016 Clinical Trials

8. Pharmacological Treatment of Presbyopia by Novel Binocularly Instilled Eye Drops: A Pilot Study. (Full text)

Pharmacological Treatment of Presbyopia by Novel Binocularly Instilled Eye Drops: A Pilot Study. The feasibility, in terms of safety and potential efficacy, of a new drug combination for binocular use as a noninvasive pharmacological solution for treating presbyopia was examined.Fourteen emmetropic presbyopic subjects (28 eyes) were given one drop of the preparation under study in each eye. For each patient, the uncorrected distance visual acuity, uncorrected near visual acuity, near and far (...) refraction, best corrected visual acuity, best corrected far-near visual acuity, photopic and scotopic pupil size, Schirmer's test, endothelial cell count, intraocular pressure, keratometry, pachymetry, and anterior chamber depth were all performed or assessed prior to the administration of the eye drops and then 0.5, 1, 2, 3, 4, and 5 h, 1 week, and 1 month post-administration prospectively in each eye and binocularly.The results showed that near uncorrected visual acuity improved by about 2-3 lines

2016 Ophthalmology and therapy PubMed

9. Instilling Eye Drops

Instilling Eye Drops Instilling Eye Drops Toggle navigation Brain Head & Neck Chest Endocrine Abdomen Musculoskeletal Skin Infectious Disease Hematology & Oncology Cohorts Diagnostics Emergency Findings Procedures Prevention & Management Pharmacy Resuscitation Trauma Emergency Procedures Ultrasound Cardiovascular Emergencies Lung Emergencies Infectious Disease Pediatrics Neurologic Emergencies Skin Exposure Miscellaneous Abuse Cancer Administration 4 Instilling Eye Drops Instilling Eye Drops (...) Aka: Instilling Eye Drops , Don't Open Eyes Technique for Eye Drop Instillation , DOT for Topical Ophthalmic , Eye Drop Technique II. Precautions Proper use of eye drops prevents systemic absorption, inaccurate dosing and medication waste Avoid touching dropper tip to eye (avoids bottle contamination) Wait at least 5 minutes before instilling another drop of the same or a different agent Allows for maximal concentration delivery of each medication drop without dilution Alternatively, may stagger

2018 FP Notebook

10. Instilling Eye Drops

Instilling Eye Drops Instilling Eye Drops Toggle navigation Brain Head & Neck Chest Endocrine Abdomen Musculoskeletal Skin Infectious Disease Hematology & Oncology Cohorts Diagnostics Emergency Findings Procedures Prevention & Management Pharmacy Resuscitation Trauma Emergency Procedures Ultrasound Cardiovascular Emergencies Lung Emergencies Infectious Disease Pediatrics Neurologic Emergencies Skin Exposure Miscellaneous Abuse Cancer Administration 4 Instilling Eye Drops Instilling Eye Drops (...) Aka: Instilling Eye Drops , Don't Open Eyes Technique for Eye Drop Instillation , DOT for Topical Ophthalmic , Eye Drop Technique II. Precautions Proper use of eye drops prevents systemic absorption, inaccurate dosing and medication waste Avoid touching dropper tip to eye (avoids bottle contamination) Wait at least 5 minutes before instilling another drop of the same or a different agent Allows for maximal concentration delivery of each medication drop without dilution Alternatively, may stagger

2018 FP Notebook

11. Effect of cooling proparacaine 0.5% eye drops on patient's comfort during instillation. (Full text)

Effect of cooling proparacaine 0.5% eye drops on patient's comfort during instillation. 25907208 2016 04 08 2018 11 13 1476-5454 29 8 2015 Aug Eye (London, England) Eye (Lond) Effect of cooling proparacaine 0.5% eye drops on patient's comfort during instillation. 1112-3 10.1038/eye.2015.59 Hu Youwei J J Department of Ophthalmology, Khoo Teck Puat Hospital, Singapore, Singapore. Chang B B Department of Ophthalmology, Khoo Teck Puat Hospital, Singapore, Singapore. eng Letter Randomized Controlled (...) Trial 2015 04 24 England Eye (Lond) 8703986 0950-222X 0 Anesthetics, Local 0 Ophthalmic Solutions B4OB0JHI1X proxymetacaine EPD1EH7F53 Propoxycaine IM Adult Anesthetics, Local administration & dosage adverse effects Double-Blind Method Eye Pain prevention & control Female Humans Male Middle Aged Ophthalmic Solutions Pain Measurement Propoxycaine administration & dosage adverse effects Prospective Studies Refrigeration Young Adult 2015 4 25 6 0 2015 4 25 6 0 2016 4 9 6 0 ppublish 25907208 eye201559

2016 Eye (London, England) PubMed

12. Inter-Rater Agreement in the Assessment of Video Recordings of Eye Drop Instillation by Glaucoma Patients (Full text)

Inter-Rater Agreement in the Assessment of Video Recordings of Eye Drop Instillation by Glaucoma Patients To create a standardized method for evaluating the video recordings of patients self-instilling eye drops and to determine the level of agreement of eye drop instillation efficacy, safety and efficiency ratings by three masked graders.Prospective cross-sectional study.78 patients with open-angle glaucoma or ocular hypertension who had at least 6 months of experience with the use of eye drop (...) medications.Participants were video recorded while self-instilling artificial tears sequentially to both eyes. Three masked observers graded these video recordings on three criteria: efficacy (the determination of whether an eye drop was instilled on the ocular surface), safety (assessment of whether the tip of the medication bottle made contact with the ocular surface or eyelids), and efficiency (the number of eye drops expressed from the bottle).After grading the video recordings based on efficacy, safety

2016 PloS one PubMed

13. A Two-Week, Randomized, Double-masked Study to Evaluate Safety and Efficacy of Lubricin (150 μg/mL) Eye Drops Versus Sodium Hyaluronate (HA) 0.18% Eye Drops (Vismed®) in Patients with Moderate Dry Eye Disease. (PubMed)

, 51.9 ± 11.8 years) or HA (N=20, 61.8 ± 13.3 years). After a saline washout period, subjects administered BID therapy for 7 days, followed by instillation as needed (2-6 drops per eye) for 7 days. Visual analog scale (VAS) including foreign body sensation, burning/stinging, itching, pain, sticky feeling, blurred vision and photophobia were primary outcomes, with secondary endpoints of corneal fluorescein staining, Schirmer test, tear film breakup time (TFBUT), eyelid and conjunctival erythema (...) A Two-Week, Randomized, Double-masked Study to Evaluate Safety and Efficacy of Lubricin (150 μg/mL) Eye Drops Versus Sodium Hyaluronate (HA) 0.18% Eye Drops (Vismed®) in Patients with Moderate Dry Eye Disease. The objective of this clinical trial (NCT02507934) was to assess the efficacy and safety of recombinant human lubricin as compared to a 0.18% sodium hyaluronate (HA) eye drop in subjects with moderate dry eye disease (DED).DEWS Grade 2-3 subjects were randomized to use lubricin (N=19

2016 The ocular surface

14. Drop instillation and glaucoma. (PubMed)

Drop instillation and glaucoma. To describe the current state of knowledge regarding glaucoma patients' eye drop technique, interventions attempting to improve eye drop technique, and methods for assessing eye drop technique.In observational studies, between 18.2 and 80% of patients contaminate their eye drop bottle by touching their eye or face, 11.3-60.6% do not instill exactly one drop, and 6.8-37.3% miss the eye with the drop. Factors significantly associated with poorer technique include (...) older age, lack of instruction on eye drop technique, female sex, arthritis, more severe visual field defect, lack of positive reinforcement to take eye drops, lower educational level, low self-efficacy, and being seen at a clinic rather than a private practice. Among intervention studies, four of five studies using a mechanical device and three of four studies using educational interventions to improve technique showed positive results, but none of the studies were randomized controlled trials.Poor

2017 Current Opinion in Ophthalmology

15. Comparison of Eye Drop Instillation Before and After Use of Drop Application Strips in Glaucoma Patients on Chronic Topical Therapy. (PubMed)

Comparison of Eye Drop Instillation Before and After Use of Drop Application Strips in Glaucoma Patients on Chronic Topical Therapy. To evaluate the impact of using drop application strips on eye drop instillation in glaucoma patients on chronic topical ocular hypotensive therapy.A total of 72 patients with primary open-angle glaucoma with an uncorrected visual acuity of 3/60 or more, self-administering topical antiglaucoma medication for >1 year were evaluated. One eye of each patient (...) was included in the study. Patients were instructed to instill 0.5% carboxymethyl cellulose drop in 1 eye. They were then instructed to instill the same drop using the drop application strips.Mean age of the patients included in the study was 50.39 ± 12.04 years. Before assistance of drop application strips, 35 (48.61%) patients placed the drop into the eye without any contact of the dropper nozzle, and, after application of the drop application strips, 66 (91.67%) patients placed the drop in the eye

2015 Journal of Glaucoma

16. Cetirizine Eye Drops for Allergic Conjunctivitis - Zerviate 1 drop twice daily

reported adverse reactions were ocular hyperemia (redness), instillation site pain, and reduction in visual acuity, which occurred in roughly 1% to 7% of patients. Treatment options for allergic conjunctivitis (eye drops) ( ). References: FDA Clears Cetirizine Eye Drops for Allergic Conjunctivitis Posted by Allergy on Labels: , No comments: Post a Comment Subscribe to: Total Pageviews About Us - : All opinions expressed here are those of their authors and not of their employer. The information provided (...) Cetirizine Eye Drops for Allergic Conjunctivitis - Zerviate 1 drop twice daily Allergy Notes: Cetirizine Eye Drops for Allergic Conjunctivitis - Zerviate 1 drop twice daily Allergy, Asthma and Immunology News Updated Daily by Board-certified Allergist at Cleveland Clinic Florida Pages Cetirizine Eye Drops for Allergic Conjunctivitis - Zerviate 1 drop twice daily The US Food and Drug Administration (FDA) approved the first topical ocular formulation of the antihistamine cetirizine

2017 Allergy Notes blog

17. Non-inferiority of Preservative-free versus BAK-preserved Latanoprost-timolol Fixed Combination Eye Drops in Patients with Open-angle Glaucoma or Ocular Hypertension. (Full text)

Non-inferiority of Preservative-free versus BAK-preserved Latanoprost-timolol Fixed Combination Eye Drops in Patients with Open-angle Glaucoma or Ocular Hypertension. Non-inferiority of efficacy was demonstrated for a preservative-free latanoprost-timolol fixed combination compared to a BAK-containing formulation at 84 days after treatment in patients with open-angle glaucoma or ocular hypertension.To compare the effect on intraocular pressure and safety of preservative-free latanoprost-timolol (...) fixed combination (T2347) to benzalkonium chloride-preserved latanoprost-timolol fixed combination in patients with open-angle glaucoma or ocular hypertension.Phase III,randomizedd, parallel-group, investigator-masked study in 10 countries. A total of 242 patients aged ≥18 years with open-angle glaucoma or ocular hypertension in both eyes controlled with a preserved latanoprost-timolol fixed combination (15.7±2.4▒mm Hg overall prior to inclusion) were randomised at Day 0 with no washout period

2019 Journal of Glaucoma PubMed

18. Noninferiority of Preservative-free Versus BAK-preserved Latanoprost-timolol Fixed Combination Eye Drops in Patients With Open-angle Glaucoma or Ocular Hypertension. (PubMed)

Noninferiority of Preservative-free Versus BAK-preserved Latanoprost-timolol Fixed Combination Eye Drops in Patients With Open-angle Glaucoma or Ocular Hypertension. PRéCIS:: Noninferiority of efficacy was demonstrated for a preservative-free latanoprost-timolol fixed combination compared with a BAK-containing formulation at 84 days after treatment in patients with open-angle glaucoma or ocular hypertension.The purpose of this study was to compare the effect on intraocular pressure and safety (...) of preservative-free latanoprost-timolol fixed combination (T2347) to benzalkonium chloride-preserved latanoprost-timolol fixed combination in patients with open-angle glaucoma or ocular hypertension.Phase III, randomized, parallel-group, investigator-masked study in 10 countries. A total of 242 patients aged 18 years or older with open-angle glaucoma or ocular hypertension in both eyes controlled with a preserved latanoprost-timolol fixed combination (15.7±2.4 mm Hg overall before inclusion) were randomized

2019 Journal of Glaucoma

19. An 8-week Study to Evaluate Safety and Efficacy of NGF Eye Drops Solution Versus Vehicle in Patients With Dry Eye

into the inferior conjunctival cul-de-sac of each eye. The patient was instructed to blink several times to thoroughly mix the fluorescein with the tear film. Change From Baseline in Wetting Distance [ Time Frame: week 8 ] The Schirmer test without anesthesia was performed to measure aqueous tear secretion prior to the instillation of any dilating or eye drops Eligibility Criteria Go to Information from the National Library of Medicine Choosing to participate in a study is an important personal decision. Talk (...) An 8-week Study to Evaluate Safety and Efficacy of NGF Eye Drops Solution Versus Vehicle in Patients With Dry Eye An 8-week Study to Evaluate Safety and Efficacy of NGF Eye Drops Solution Versus Vehicle in Patients With Dry Eye - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved

2017 Clinical Trials

20. A Study to Evaluate the Performance and Safety of CBL-102 Versus Vismed® Multi Eye Drops in the Management of Dry Eye

, burning, stinging, itching, blurred vision, sensitivity to light, each graded from 0 to 4 Schirmer test [ Time Frame: Baseline (Day 0), Visit 4 (Day 28) ] Mean CFB in the study eye in volume of tear fluid secretion as assessed by the unanaesthetized Schirmer test Questionnaire of daily frequency of instillations [ Time Frame: through study completion, an average of 3 months ] Daily frequency of investigational eye drop instillations as reported in subject diary Other Outcome Measures: Adverse events (...) A Study to Evaluate the Performance and Safety of CBL-102 Versus Vismed® Multi Eye Drops in the Management of Dry Eye A Study to Evaluate the Performance and Safety of CBL-102 Versus Vismed® Multi Eye Drops in the Management of Dry Eye - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number

2017 Clinical Trials

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