Clinical Trials Logo

Clinical Trial Summary

Given the current lack of satisfactory options for the management of IUD insertion pain, could the virtual reality headset be an innovative and effective tool? The objective is to compare the pain experienced during IUD insertion between a group of women wearing a virtual reality helmet and a group not wearing one. Observational, prospective, randomized, open-label, monocentric study.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04539899
Study type Interventional
Source Rennes University Hospital
Contact
Status Completed
Phase N/A
Start date September 23, 2020
Completion date April 29, 2022

See also
  Status Clinical Trial Phase
Recruiting NCT03868137 - Multi-dose Ibuprofen Prophylaxis for IUD-insertion N/A
Recruiting NCT06023849 - Trans Caesarean Intra Uterine Contraceptive Device Insertion Versus Conventional Postpartum 6 Weeks Insertion N/A
Completed NCT04932382 - Misoprostol Prior to Intrauterine Device Insertion N/A
Active, not recruiting NCT04927741 - Essential Oils Following IUD Insertion N/A
Completed NCT05383924 - Intrauterine Contraceptive Device Insertion During Cesarean Section (CS) Versus Delayed Insertion N/A
Completed NCT04389021 - Virtual Reality Simulation for Intrauterine Device Insertion: A Randomized Clinical Trial N/A
Completed NCT05187078 - Allis Clamp Versus Single-tooth Tenaculum N/A
Recruiting NCT05339555 - IUD Self-Removal Study N/A
Completed NCT04379102 - The Role Of Local Anesthetics in the Management of Adverse Effects Associated With Intrauterine Device Application
Recruiting NCT05875571 - Intravenous Ketorolac Administration to Attenuate Post-procedural Pain Associated With Intrauterine Device Placement Phase 4
Active, not recruiting NCT02076217 - Quick Start of Highly Effective Contraception
Recruiting NCT05700812 - IUD Placement Without Sounding N/A
Recruiting NCT05252117 - Uterovaginal Plexus Block With Articaine for Intrauterine Device Placement Patients Who Are Indicated for the Use of Copper IUD as a Contraceptive Method Will be Invited to Participate in This Research. Phase 4
Not yet recruiting NCT05471362 - Barriers of Immediate Postpartum Intrauterine Device Uptake
Not yet recruiting NCT04630548 - Safety and Efficacy of Immediate Post Placental IUD Insertion in Patients Undergoing Cesarean Delivery N/A
Not yet recruiting NCT05283798 - Insertion of Copper T380 Versus Multiload IUD Post Partum N/A
Not yet recruiting NCT06240260 - TENS Unit for Analgesia During IUD Insertion N/A
Completed NCT06042556 - IUD Self-Removal: Evaluating an Online Guide for Self-removal in Clinical and Non-clinical Settings N/A