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Diphenhydramine

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61. Diphenhydramine as an Adjunctive Sedative in Patients on Chronic Opioids

Diphenhydramine as an Adjunctive Sedative in Patients on Chronic Opioids Diphenhydramine as an Adjunctive Sedative in Patients on Chronic Opioids - 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 (...) . Diphenhydramine as an Adjunctive Sedative in Patients on Chronic Opioids 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. Read our for details. ClinicalTrials.gov Identifier: NCT01967433 Recruitment Status : Unknown Verified April 2017 by University of Oklahoma. Recruitment status was: Active, not recruiting First Posted : October 22, 2013 Last Update Posted : April

2013 Clinical Trials

62. Next-Day Residual Effects of Gabapentin, Diphenhydramine and Triazolam on Simulated Driving Performance in Normal Volunteers

Next-Day Residual Effects of Gabapentin, Diphenhydramine and Triazolam on Simulated Driving Performance in Normal Volunteers Next-Day Residual Effects of Gabapentin, Diphenhydramine and Triazolam on Simulated Driving Performance in Normal Volunteers - 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. Next-Day Residual Effects of Gabapentin, Diphenhydramine and Triazolam on Simulated Driving Performance in Normal Volunteers 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. Read our for details. ClinicalTrials.gov Identifier: NCT01888497 Recruitment Status

2013 Clinical Trials

63. Randomized Trial of Diphenhydramine Versus Continued Midazolam in "Difficult-to-sedate" Patients Undergoing Colonoscopy

Randomized Trial of Diphenhydramine Versus Continued Midazolam in "Difficult-to-sedate" Patients Undergoing Colonoscopy Randomized Trial of Diphenhydramine Versus Continued Midazolam in "Difficult-to-sedate" Patients Undergoing Colonoscopy - 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. Randomized Trial of Diphenhydramine Versus Continued Midazolam in "Difficult-to-sedate" Patients Undergoing Colonoscopy 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. Read our for details. ClinicalTrials.gov Identifier: NCT01769586 Recruitment Status : Completed First

2013 Clinical Trials

64. Diphenhydramine and Acute Kidney Injury (PubMed)

Diphenhydramine and Acute Kidney Injury Seldom considered to be a drug that causes renal problems, diphenhydramine can have adverse effects in some patients, as illustrated by a case study of a middle-aged veteran. Extra precautions are urged before this medication is prescribed, especially in elderly patients.

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2013 Pharmacy and Therapeutics

65. A trial of midazolam vs diphenhydramine in prophylaxis of metoclopramide-induced akathisia. (PubMed)

A trial of midazolam vs diphenhydramine in prophylaxis of metoclopramide-induced akathisia. The study aimed to evaluate the effects of midazolam and diphenhydramine for the prevention of metoclopramide-induced akathisia.This randomized, double-blind, and controlled trial aimed to investigate coadministered midazolam vs diphenhydramine in the prophylaxis of metoclopramide-induced akathisia. Patients 18 to 65 years of age who presented to the emergency department with primary or secondary (...) complaints of nausea and/or moderate to severe vascular-type headache were eligible for this study. Patients were randomized to one of the fallowing 3 groups: (1) metoclopramide 10 mg + midazolam 1.5 mg; (2) metoclopramide 10 mg + diphenhydramine 20 mg; (3) metoclopramide 10 mg + placebo. Metoclopramide was administered as a 2-minute bolus infusion. Midazolam, diphenhydramine, and normal saline solution were administered as a 15-minute slow infusion. The whole procedure was observed; and akathisia

2012 American Journal of Emergency Medicine

66. [Prophylactic effect of diphenhydramine on postoperative vomiting in children after laparoscopic surgery]. (PubMed)

[Prophylactic effect of diphenhydramine on postoperative vomiting in children after laparoscopic surgery]. Laparoscopic percutaneous extraperitoneal closure (LPEC), introduced as an alternative to a conventional open inguinal hernia repair in children, has shown a higher incidence of postoperative vomiting (POV). The aim of this study was to examine whether a prophylactic use of diphenhydramine can decrease the incidence of POV in children undergoing LPEC.We studied 60 girls between 1 and 6 (...) years of age with ASA physical status I or II undergoing LPEC. Patients were allocated to receive either diphenhydramine 1 mg x kg(-1) intravenously (n = 30) or placebo (n = 30) during the operation. Anesthesia was performed with air-oxygen-sevoflurane in combination with epidural anesthesia. Opioids were avoided throughout the perioperative period. The incidence of POV was recorded postoperatively.Demographic data were similar between the groups. The overall incidence of POV during the first 24

2012 Masui. The Japanese journal of anesthesiology

67. Lorazepam, Diphenhydramine Hydrochloride, and Haloperidol Gel in Patients With Nausea

Lorazepam, Diphenhydramine Hydrochloride, and Haloperidol Gel in Patients With Nausea Randomized Trial of the Effectiveness of Topical "ABH Gel" vs. Placebo in Cancer Patients With Nausea - 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 (...) Update Posted : October 16, 2015 Sponsor: Virginia Commonwealth University Collaborator: National Cancer Institute (NCI) Information provided by (Responsible Party): Virginia Commonwealth University Study Details Study Description Go to Brief Summary: This randomized clinical trial studies ABH (lorazepam, diphenhydramine hydrochloride, and haloperidol) gel in patients with nausea. ABH gel, when absorbed into the skin, may be an effective treatment for nausea and vomiting. The general purpose

2012 Clinical Trials

68. Diphenhydramine

Diphenhydramine Diphenhydramine 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 Diphenhydramine Diphenhydramine Aka: Diphenhydramine (...) , Benadryl From Related Chapters II. Indications See for Allergy III. Dosing: Standard Adult: 25-50 mg PO/IV/IM q6h Child: 5 mg/kg/day divided qid (12.5 mg/5 ml) IV. Preparation: Diphenhydramine 1% (for Local Anesthesia) Dilute Diphenhydramine 5% in (1:4) Longer delay to onset of action than Shorter duration of action than Images: Related links to external sites (from Bing) These images are a random sampling from a Bing search on the term "Diphenhydramine." Click on the image (or right click) to open

2015 FP Notebook

69. Comparison of cetirizine and diphenhydramine in the treatment of acute food-induced allergic reactions. (PubMed)

Comparison of cetirizine and diphenhydramine in the treatment of acute food-induced allergic reactions. 21945608 2011 12 12 2018 11 13 1097-6825 128 5 2011 Nov The Journal of allergy and clinical immunology J. Allergy Clin. Immunol. Comparison of cetirizine and diphenhydramine in the treatment of acute food-induced allergic reactions. 1127-8 10.1016/j.jaci.2011.08.026 Park Joon H JH Godbold James H JH Chung Danna D Sampson Hugh A HA Wang Julie J eng RR026134 RR NCRR NIH HHS United States (...) Allergy Clin Immunol 1275002 0091-6749 0 Anti-Allergic Agents 0 Hypnotics and Sedatives 8GTS82S83M Diphenhydramine YO7261ME24 Cetirizine AIM IM Acute Disease Adolescent Anti-Allergic Agents therapeutic use Cetirizine therapeutic use Child Child, Preschool Diphenhydramine therapeutic use Food Hypersensitivity drug therapy Humans Hypnotics and Sedatives Young Adult 2011 03 30 2011 08 19 2011 08 31 2011 9 28 6 0 2011 9 29 6 0 2011 12 14 6 0 ppublish 21945608 S0091-6749(11)01392-3 10.1016/j.jaci

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2011 The Journal of allergy and clinical immunology

70. Evaluation of the subjective and reinforcing effects of diphenhydramine, levetiracetam, and valproic acid. (PubMed)

Evaluation of the subjective and reinforcing effects of diphenhydramine, levetiracetam, and valproic acid. Few unscheduled sedating medications have been evaluated for their subjective and reinforcing effects in humans. To increase the information available about unscheduled sedating medications and to evaluate the ability of human laboratory measures to discriminate between scheduled and unscheduled sedating drugs, 24 subjects with a history of experience with several classes of drugs of abuse (...) , including sedatives and/or alcohol, and who reported liking a test dose of pentobarbital 300 mg, were randomized to single doses of diphenhydramine 400 mg, levetiracetam 4000 mg, valproic acid 1500 mg, diazepam 30 mg or placebo in a double-blind, 5-way crossover study. On the Addiction Research Center Inventory-Morphine-Benzedrine Group and the Next Day Questionnaire measures 'Take Again' and 'Willing to Pay', diazepam produced a significantly greater effect than placebo; all three other active drugs

2011 Journal of psychopharmacology (Oxford, England)

71. Efficacy of intramuscular nalbuphine versus diphenhydramine for the prevention of epidural morphine-induced pruritus after cesarean delivery. (PubMed)

Efficacy of intramuscular nalbuphine versus diphenhydramine for the prevention of epidural morphine-induced pruritus after cesarean delivery. Pruritus is the most common side effect of epidural morphine analgesia. Diphenhydramine is a widely used agent for the treatment of urticarial pruritus. Nalbuphine is a mixed opioid agonist-antagonist and has been reported to be effective in treating opioid-induced pruritus. We compared the effectiveness of intramuscular diphenhydramine and nalbuphine (...) for the prevention of epidural morphine-induced pruritus after cesarean section.One hundred and fifty, American Society of Anesthesiologists physical status I or II, women undergoing cesarean section with epidural anesthesia were randomly assigned to three groups. Group S, group D, and group N received intramuscular normal saline (1 ml; n = 50), diphenhydramine (30 mg/1 ml; n = 50), and nalbuphine (10 mg/1 ml; n = 50), respectively, after delivery of the baby. The occurrence and the severity of pruritus were

2011 Chang Gung medical journal

72. Motion sickness: comparison of metoclopramide and diphenhydramine to placebo. (PubMed)

Motion sickness: comparison of metoclopramide and diphenhydramine to placebo. This is an evaluation of the efficacy of metoclopramide (MTCP) or diphenhydramine (DPH) to relieve symptoms of motion sickness in patients being transported via ambulance in a mountainous setting.This is a prospective, randomized, double-blinded, placebo-controlled study of patients transported by ambulance in the Sierra Nevada mountains of Fresno County. Consenting patients who met the inclusion criteria were asked (...) groups.During ambulance transport in a mountainous setting, the administration of MTCP is superior to both DPH and placebo in the treatment of motion sickness. Diphenhydramine is not superior to placebo.

2011 Prehospital and disaster medicine

73. Evaluate Analgesic/Sedative Efficacy of Naproxen Sodium and Diphenhydramine in Patients With Postsurgical Dental Pain

Evaluate Analgesic/Sedative Efficacy of Naproxen Sodium and Diphenhydramine in Patients With Postsurgical Dental Pain Evaluate Analgesic/Sedative Efficacy of Naproxen Sodium and Diphenhydramine in Patients With Postsurgical Dental Pain - 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. Evaluate Analgesic/Sedative Efficacy of Naproxen Sodium and Diphenhydramine in Patients With Postsurgical Dental Pain (Morpheus II) 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. Read our for details. ClinicalTrials.gov Identifier: NCT01280591 Recruitment Status : Completed First

2011 Clinical Trials

74. Influence of Losartan and Diphenhydramine on Emotional and Cognitive Functions in Healthy Human Subjects

Influence of Losartan and Diphenhydramine on Emotional and Cognitive Functions in Healthy Human Subjects Influence of Losartan and Diphenhydramine on Emotional and Cognitive Functions in Healthy Human Subjects - 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. Influence of Losartan and Diphenhydramine on Emotional and Cognitive Functions in Healthy Human Subjects (LoDi-Basel) 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. Read our for details. ClinicalTrials.gov Identifier: NCT01321021 Recruitment Status : Completed First Posted : March 23, 2011 Last Update

2011 Clinical Trials

75. Safety Trial of Naproxen Sodium/ Diphenhydramine

Safety Trial of Naproxen Sodium/ Diphenhydramine Safety Trial of Naproxen Sodium/ Diphenhydramine - 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. Safety Trial of Naproxen Sodium/ Diphenhydramine (MUST (...) : The purpose of this trial is to see how safe the combination of naproxen sodium 440 mg and diphenhydramine hydrochloride (DPH) 50 mg (the investigational product) is compared to placebo (capsules containing no drug) when taken for 10 days. Condition or disease Intervention/treatment Phase Pain Drug: Naproxen sodium 440 mg/DPH 50 mg (BAY98-7111) Drug: Placebo Phase 3 Study Design Go to Layout table for study information Study Type : Interventional (Clinical Trial) Actual Enrollment : 326 participants

2011 Clinical Trials

76. Therapeutic Effects of "Ibuprofen, Diphenhydramine and Aluminium MgS" on Recurrent Aphthous Stomatitis

Therapeutic Effects of "Ibuprofen, Diphenhydramine and Aluminium MgS" on Recurrent Aphthous Stomatitis Therapeutic Effects of "Ibuprofen, Diphenhydramine and Aluminium MgS" on Recurrent Aphthous Stomatitis - 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. Therapeutic Effects of "Ibuprofen, Diphenhydramine and Aluminium MgS" on Recurrent Aphthous Stomatitis 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. Read our for details. ClinicalTrials.gov Identifier: NCT01293968 Recruitment Status : Completed First Posted : February 11, 2011 Results First Posted : June 20

2011 Clinical Trials

77. Pharmacogenetic Factors and Side Effects of Metoclopramide and Diphenhydramine

Pharmacogenetic Factors and Side Effects of Metoclopramide and Diphenhydramine Pharmacogenetic Factors and Side Effects of Metoclopramide and Diphenhydramine - 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 (...) . Pharmacogenetic Factors and Side Effects of Metoclopramide and Diphenhydramine (MalD) 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. Read our for details. ClinicalTrials.gov Identifier: NCT01289938 Recruitment Status : Terminated (To unsuccessful recruitment of rare UM-genotype. All other planned genotype groups are completed (EM, IM and PM).) First Posted

2011 Clinical Trials

78. A Dose Ranging Effect of Preoperative Diphenhydramine on Postoperative Quality of Recovery After Ambulatory Surgery

A Dose Ranging Effect of Preoperative Diphenhydramine on Postoperative Quality of Recovery After Ambulatory Surgery A Dose Ranging Effect of Preoperative Diphenhydramine on Postoperative Quality of Recovery After Ambulatory Surgery - 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 Dose Ranging Effect of Preoperative Diphenhydramine on Postoperative Quality of Recovery After Ambulatory Surgery 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. Read our for details. ClinicalTrials.gov Identifier: NCT01451762 Recruitment Status : Completed First Posted : October

2011 Clinical Trials

79. Evaluate Analgesic / Sedative Efficacy of Naproxen Sodium and Diphenhydramine in Patients With Postsurgical Dental Pain

Evaluate Analgesic / Sedative Efficacy of Naproxen Sodium and Diphenhydramine in Patients With Postsurgical Dental Pain Evaluate Analgesic / Sedative Efficacy of Naproxen Sodium and Diphenhydramine in Patients With Postsurgical Dental Pain - 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. Evaluate Analgesic / Sedative Efficacy of Naproxen Sodium and Diphenhydramine in Patients With Postsurgical Dental Pain (Morpheus/DPH) 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. Read our for details. ClinicalTrials.gov Identifier: NCT01495858 Recruitment Status

2011 Clinical Trials

80. Case Files of the Medical Toxicology Fellowship at Drexel University: Rhabdomyolysis and Compartment Syndrome Following Acute Diphenhydramine Overdose (PubMed)

Case Files of the Medical Toxicology Fellowship at Drexel University: Rhabdomyolysis and Compartment Syndrome Following Acute Diphenhydramine Overdose 21656083 2011 11 30 2018 11 13 1937-6995 7 3 2011 Sep Journal of medical toxicology : official journal of the American College of Medical Toxicology J Med Toxicol Case files of the medical toxicology fellowship at Drexel University. Rhabdomyolysis and compartment syndrome following acute diphenhydramine overdose. 213-9 10.1007/s13181-011-0157-3 (...) Vearrier David D Division of Medical Toxicology, Department of Emergency Medicine, Drexel University College of Medicine, Philadelphia, PA 19102, USA. david.vearrier@drexelmed.edu Curtis John A JA eng Case Reports Journal Article United States J Med Toxicol 101284598 1556-9039 0 Central Nervous System Depressants 0 Histamine H1 Antagonists 0 Xenobiotics 3K9958V90M Ethanol 8GTS82S83M Diphenhydramine IM Adult Blood Chemical Analysis Central Nervous System Depressants poisoning Compartment Syndromes

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2011 Journal of Medical Toxicology

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