How to Trip Rapid Review

Step 1: Select articles relevant to your search (remember the system is only optimised for single intervention studies)

Step 2: press

Step 3: review the result, and maybe amend the or if you know better! If we're unsure of the overall sentiment of the trial we will display the conclusion under the article title. We then require you to tell us what the correct sentiment is.

11,699 results for

Intrauterine Device

by
...
Latest & greatest
Alerts

Export results

Use check boxes to select individual results below

SmartSearch available

Trip's SmartSearch engine has discovered connected searches & results. Click to show

181. Immediate Postpartum Intrauterine Contraceptive Device Insertions in Caesarean and Vaginal Deliveries: A Comparative Study of Follow-Up Outcomes (PubMed)

Immediate Postpartum Intrauterine Contraceptive Device Insertions in Caesarean and Vaginal Deliveries: A Comparative Study of Follow-Up Outcomes Background. Immediate postpartum intrauterine contraceptive device (IPPIUCD) is a lucrative postpartum family planning method which provides effective reversible contraception to women in the delivery setting. Our aim was to study the clinical outcomes of IPPIUCD insertions and compare them as a factor of route of insertion (vaginal versus caesarean

Full Text available with Trip Pro

2016 International journal of reproductive medicine

182. Migration of an intrauterine device to the left inguinal region, the first reported case (PubMed)

Migration of an intrauterine device to the left inguinal region, the first reported case A large number of complications are reported with the use of IUD. Migration to inguinal region has not been mentioned in literature. We report a rare case of migrated IUD to inguinal canal.A 25-year-old lady presented with a painfull mass in the left inguinal region. Diagnostic work up showed migrated IUD to inguinal region. Operation was done and the impacted IUD with surrounding granuloma

Full Text available with Trip Pro

2016 International journal of surgery case reports

183. Translocation of Postplacental Intrauterine Device: A Rare Complication (PubMed)

Translocation of Postplacental Intrauterine Device: A Rare Complication 27803550 2018 11 13 0971-9202 66 Suppl 2 2016 10 Journal of obstetrics and gynaecology of India J Obstet Gynaecol India Translocation of Postplacental Intrauterine Device: A Rare Complication. 707-709 Mishra Sujnanendra S 0000-0003-1003-9884 Balangir, Odisha India. eng Journal Article 2016 04 27 India J Obstet Gynaecol India 0374763 0975-6434 The authors declare that there are no competing interests. Ethical Statement

Full Text available with Trip Pro

2016 Journal of obstetrics and gynaecology of India

184. Is There Any Impact of Copper Intrauterine Device on Female Sexual Functioning? (PubMed)

Is There Any Impact of Copper Intrauterine Device on Female Sexual Functioning? Intrauterine Device (IUD) is the most preferred modern contraceptive method in Turkey. Female Sexual Dysfunction (FSD) is defined as lack of one or more of the components in the sexual response cycle which includes sexual desire, impaired arousal and inability achieving an orgasm or pain with intercourse. FSD has multi-factorial aetiology. Advanced age and menopause, fatigue and stress, psychiatric and neurologic

Full Text available with Trip Pro

2016 Journal of clinical and diagnostic research : JCDR

185. Evaluation of a Novel and Simplified Technique for Intrauterine Contraceptive Devices Insertion: a Prospective Cohort Study

Evaluation of a Novel and Simplified Technique for Intrauterine Contraceptive Devices Insertion: a Prospective Cohort Study Evaluation of a Novel and Simplified Technique for Intrauterine Contraceptive Devices Insertion: a Prospective Cohort Study - 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 Novel and Simplified Technique for Intrauterine Contraceptive Devices Insertion: a Prospective Cohort Study 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: NCT02841826 Recruitment Status

2016 Clinical Trials

186. Evaluation of a Novel Technique for Intrauterine Contraceptive Devices Insertion

Evaluation of a Novel Technique for Intrauterine Contraceptive Devices Insertion Evaluation of a Novel Technique for Intrauterine Contraceptive Devices Insertion - 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 Novel Technique for Intrauterine Contraceptive Devices Insertion 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: NCT02842177 Recruitment Status : Completed First Posted : July 22, 2016 Last Update Posted : March 28, 2017 Sponsor: Assiut University Information provided

2016 Clinical Trials

187. Cold Compress for Pain Associated With Intrauterine Device Insertion

Cold Compress for Pain Associated With Intrauterine Device Insertion Cold Compress for Pain Associated With Intrauterine Device Insertion - 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. Cold Compress (...) for Pain Associated With Intrauterine Device Insertion 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: NCT02898831 Recruitment Status : Completed First Posted : September 13, 2016 Last Update Posted : March 18, 2019 Sponsor: Virginia Commonwealth University Information provided by (Responsible Party

2016 Clinical Trials

188. Comparison Between 2 Doses of Misoprostol Before Intrauterine Device

Comparison Between 2 Doses of Misoprostol Before Intrauterine Device Comparison Between 2 Doses of Misoprostol Before Intrauterine Device - 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. Comparison Between 2 (...) Doses of Misoprostol Before Intrauterine Device 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: NCT02901561 Recruitment Status : Completed First Posted : September 15, 2016 Last Update Posted : March 14, 2017 Sponsor: Assiut University Information provided by (Responsible Party): Ahmed Mohamed Abbas

2016 Clinical Trials

189. Indomethacin Use in Pain Relief During Intrauterine Device Insertion

Indomethacin Use in Pain Relief During Intrauterine Device Insertion Indomethacin Use in Pain Relief During Intrauterine Device Insertion - 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. Indomethacin Use (...) in Pain Relief During Intrauterine Device Insertion (INDO-IUD) 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: NCT02711358 Recruitment Status : Completed First Posted : March 17, 2016 Last Update Posted : November 29, 2016 Sponsor: Assiut University Information provided by (Responsible Party): Ahmed

2016 Clinical Trials

190. Expulsion of Immediate Postplacental Copper Intrauterine Devices at Six Months: A Prospective Cohort Study

Expulsion of Immediate Postplacental Copper Intrauterine Devices at Six Months: A Prospective Cohort Study Expulsion of Immediate Postplacental Copper Intrauterine Devices at Six Months: A Prospective Cohort Study - 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. Expulsion of Immediate Postplacental Copper Intrauterine Devices at Six Months: A Prospective Cohort Study (PPIUD) 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: NCT02706340 Recruitment Status : Completed First Posted : March 11, 2016 Last Update

2016 Clinical Trials

191. Oral Diclofenac Sodium Versus Oral Hyoscine Butyl Bromide During Intrauterine Device Insertion

Oral Diclofenac Sodium Versus Oral Hyoscine Butyl Bromide During Intrauterine Device Insertion Oral Diclofenac Sodium Versus Oral Hyoscine Butyl Bromide During Intrauterine Device Insertion - 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. Oral Diclofenac Sodium Versus Oral Hyoscine Butyl Bromide During Intrauterine Device Insertion 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: NCT02714231 Recruitment Status : Completed First Posted : March 21, 2016 Last Update Posted : July 19, 2017 Sponsor: Assiut

2016 Clinical Trials

192. A Study to Compare the Menstrual Bleeding Profile Among Jaydess® and Copper Intrauterine Device (IUD) Users. COLIBRI STUDY (Copper and Levonorgestrel IUD Barcelona Research Initiative).

A Study to Compare the Menstrual Bleeding Profile Among Jaydess® and Copper Intrauterine Device (IUD) Users. COLIBRI STUDY (Copper and Levonorgestrel IUD Barcelona Research Initiative). A Study to Compare the Menstrual Bleeding Profile Among Jaydess® and Copper Intrauterine Device (IUD) Users. COLIBRI STUDY (Copper and Levonorgestrel IUD Barcelona Research Initiative). - 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 to Compare the Menstrual Bleeding Profile Among Jaydess® and Copper Intrauterine Device (IUD) Users. COLIBRI STUDY (Copper and Levonorgestrel IUD Barcelona Research Initiative). (COLIBRI) The safety and scientific validity of this study is the responsibility of the study sponsor

2016 Clinical Trials

193. Efficacy of Ketoprofen Before Intrauterine Device Insertion

Efficacy of Ketoprofen Before Intrauterine Device Insertion Efficacy of Ketoprofen Before Intrauterine Device Insertion - 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 of Ketoprofen Before (...) Intrauterine Device Insertion 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: NCT02905058 Recruitment Status : Completed First Posted : September 19, 2016 Last Update Posted : November 14, 2017 Sponsor: Assiut University Information provided by (Responsible Party): Ahmed Mohamed Abbas, Assiut University Study

2016 Clinical Trials

194. Comparison Between Intrauterine Contraceptive Device Insertion During Cesarean Section Vs Conventional Application

Comparison Between Intrauterine Contraceptive Device Insertion During Cesarean Section Vs Conventional Application Comparison Between Intrauterine Contraceptive Device Insertion During Cesarean Section Vs Conventional Application - 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. Comparison Between Intrauterine Contraceptive Device Insertion During Cesarean Section Vs Conventional Application 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: NCT02674139 Recruitment Status : Unknown Verified September 2016

2016 Clinical Trials

195. The Effect of Intrauterine Devices on Acquisition and Clearance of Human Papillomavirus. (PubMed)

The Effect of Intrauterine Devices on Acquisition and Clearance of Human Papillomavirus. Previous studies have shown a decrease in cervical cancer associated with intrauterine device use. It has been hypothesized that intrauterine device use may alter the natural history of human papillomavirus infections, preempting development of precancerous lesions of the cervix and cervical cancer, but the effect of intrauterine devices on the natural history of human papillomavirus infection (...) and subsequent development of cervical cancer is poorly understood.The purpose of this study was to evaluate the association between intrauterine device use and cervical high-risk human papillomavirus acquisition and clearance.This is a prospective cohort study conducted from October 2000 through June 2014 among 676 sexually active young women and girls enrolled from family planning clinics in San Francisco, CA. Data were analyzed using a Cox proportional hazards model, including time-varying indicators

Full Text available with Trip Pro

2016 American Journal of Obstetrics and Gynecology

196. Chronic vulvovaginal candidiasis in patients using a levonorgestrel-containing intrauterine device. (PubMed)

Chronic vulvovaginal candidiasis in patients using a levonorgestrel-containing intrauterine device. Chronic vulvovaginal candidiasis is usually responsive to therapy with oral antifungals. We present a case series of 13 patients with this condition who were also using a levonorgestrel intrauterine system (LNG-IUS). All cases responded to ongoing oral fluconazole therapy while the LNG-IUS was in situ. The LNG-IUS was removed in six patients and of these, two experienced clinical improvement

2016 Australasian Journal of Dermatology

197. Intrauterine Device Insertion Failure After Misoprostol Administration: A Systematic Review. (PubMed)

Intrauterine Device Insertion Failure After Misoprostol Administration: A Systematic Review. To examine rates of intrauterine device (IUD) insertion failure with and without prior misoprostol administration. Additional outcomes included difficulty of insertion, subjective pain, expulsion, and complications.Systematic searches were performed in PubMed MEDLINE, Cochrane Central Register of Controlled Trials, ClinicalTrials.gov, and Cumulative Index to Nursing and Allied Health Literature (...) for articles with the following keywords: "misoprostol," "intrauterine devices," and "IUDs."A total of 161 unique results were retrieved. Titles, abstracts, and full-text articles were independently screened twice by two reviewers for content and relevance. Quality assessment was performed using previously established criteria. After screening and quality assessment, nine randomized controlled trials (RCTs) were obtained for inclusion. Six articles were designated high quality and three were designated low

2016 Obstetrics and Gynecology

198. New developments in long-acting reversible contraception: the promise of intrauterine devices and implants to improve family planning services. (PubMed)

New developments in long-acting reversible contraception: the promise of intrauterine devices and implants to improve family planning services. After decades of having the developed world's highest rates of unintended pregnancy, the United States finally shows signs of improvement. This progress is likely due in large part to increased use of highly effective long-acting reversible methods of contraception. These methods can be placed and do not require any maintenance to provide years

2016 Fertility and Sterility

199. Use of effective contraception six months after emergency contraception with a copper intrauterine device or ulipristal acetate - a prospective observational cohort study. (PubMed)

Use of effective contraception six months after emergency contraception with a copper intrauterine device or ulipristal acetate - a prospective observational cohort study. Emergency contraception must be followed by the use of an effective method of contraception in order to reduce future risk of unintended pregnancies. Provision of long-acting reversible contraception (LARC) is highly effective in this regard. The aim of our study was to compare use of an effective method of contraception 6 (...) months following insertion of a copper intrauterine device (Cu-IUD) or intake of ulipristal acetate (UPA) for emergency contraception (EC).Women (n = 79) presenting with need for EC at an outpatient midwifery clinic chose either Cu-IUD or UPA according to preference. Follow up was 3 and 6 months later through telephone interviews. Primary outcome was use of an effective contraceptive method at the 6-month follow up. Secondary outcomes included use of an effective contraceptive method at 3 months

2016 Acta Obstetricia et Gynecologica Scandinavica

200. Use of intrauterine devices in nulliparous women. (PubMed)

Use of intrauterine devices in nulliparous women. Five intrauterine devices (IUDs) are available in the United States: four levonorgestrel-releasing intrauterine systems (two containing 52 mg, one containing 19.5 mg and one containing 13.5 mg) and one copper-bearing device (Copper T 380A). All IUDs have very low typical-use failure rates and high acceptability ratings, yet they are used by a minority of women, with nulliparous women less likely to do so than parous women. The objective (...) of this clinical review is to give evidence-based recommendations for the use of IUDs in nulliparous women. Intrauterine devices are safe and effective for the majority of women including those who are nulliparous, and should be routinely included in the contraception options offered to them.Copyright © 2016 Elsevier Inc. All rights reserved.

2016 Contraception

To help you find the content you need quickly, you can filter your results via the categories on the right-hand side >>>>