Clinical Trials Logo
  1. Home
  2. IUD
  3. NCT05187078

Allis Clamp Versus Single-tooth Tenaculum

IUD Clinical Trial

Official title:
Cervical Bleeding With Cervical Stabilization During IUD Placement: Allis Clamp Versus Single-tooth Tenaculum

Clinical Trial Summary

This study aims to determine whether an Allis clamp is an effective clamp for cervical stabilization compared to a single-tooth tenaculum.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05187078
Study type Interventional
Source University of Kentucky
Contact
Status Completed
Phase N/A
Start date March 1, 2017
Completion date March 1, 2018
View Details
See also
  Status Clinical Trial Phase
Recruiting NCT03868137 - Multi-dose Ibuprofen Prophylaxis for IUD-insertion N/A
Completed NCT04539899 - Evaluation of the Influence of the Virtual Reality Helmet on Pain During 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
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