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IUD Insertion Complication clinical trials

View clinical trials related to IUD Insertion Complication.

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NCT ID: NCT05594108 Completed - Clinical trials for IUD Insertion Complication

Ultrasound-guided IUD Insertion During Family Medicine Residency Training

Start date: July 15, 2020
Phase: N/A
Study type: Interventional

The objective of this pilot study is to test that hypothesis that ultrasound guided IUD placement by family medicine residents improves patient pain scores, procedure completion time, and procedure complication rates. The secondary objective is to test the hypothesis that ultrasound guided IUD placement improves resident confidence in performing the procedure. A prospective, randomized controlled pilot study will be conducted in the Department of Academic Family Medicine at the University of Saskatchewan. All women undergoing IUD placement (hormonal or non-hormonal) at West Winds Primary Care Center from Mar 1, 2020- Mar 1, 2021 will be invited to participate. Informed consent will be obtained from each patient and the resident inserting the IUD prior to initiating study procedures. The control group will comprise 20 women undergoing non-ultrasound guided IUD placement. The experimental group will comprise 20 women undergoing transabdominal ultrasound guided IUD placement. Patient pain scores and resident confidence scores will be tabulated using likert scales and compared between control and experimental groups using independent sample t-tests. Procedure completion time (minutes) will be compared between groups using t-tests. Procedure complications rates will be categorized as: a) inability to penetrate the cervix, b) improper location, c) inability to release the IUD from the insertion device, d) perforation, e) vasovagal reactions, and f) post-procedure infection; outcomes will be compared between groups using Chi-square analyses.

NCT ID: NCT04963582 Completed - Acute Pain Clinical Trials

LI4 Acupuncture for Analgesia in Intrauterine Device Insertion

Start date: July 5, 2021
Phase: N/A
Study type: Interventional

Pain during IUD insertion is substantially psychologic in origin, responds extremely well to non-pharmacologic interventions. Considering the fact that acupuncture is a modality exerting both psychologic and physiologic effects, the authors presume that acupuncture administration before IUD insertion may have positive effects on pain control. From this point of view, the aim of this study to investigate the effects of LI4 acupuncture administered shortly before IUD insertion on pain perception and discomfort of the women.

NCT ID: NCT04080336 Completed - Clinical trials for IUD Insertion Complication

Comparison of Vaginal Misoprostol and Dinoprostone Prior to Copper Intrauterine Device Insertion in Nulliparous Women

Start date: September 10, 2019
Phase: Phase 4
Study type: Interventional

To compare the effect of vaginal dinoprostone versus vaginal misoprostol administered before the copper intrauterine device(IUD) insertion in reducing IUD inertion pain and the difficulty in inserting the IUD in nulliparous women.

NCT ID: NCT03111342 Completed - Pain, Acute Clinical Trials

Intracervical Anesthesia and Pain Associated With Intrauterine Contraceptive Insertion

Start date: June 1, 2017
Phase: Phase 4
Study type: Interventional

The primary aim of our study is to evaluate the effect of intracervical anesthesia on pain scores immediately following levonorgestrel-releasing intrauterine system (LNG-IUS) insertion in nulligravida women.

NCT ID: NCT02716636 Completed - Clinical trials for Endometrial Diseases

Fast Versus Slow Tenaculum Placement

Start date: April 11, 2016
Phase: N/A
Study type: Interventional

The purpose of the study is to investigate whether the speed of tenaculum placement affects perceived patient pain during office transcervical procedures.