Patient-Applied Pretreatment Analgesia for Intrauterine Device Placement - Trial NCT05890495
Access comprehensive clinical trial information for NCT05890495 through Pure Global AI's free database. This Phase 4 trial is sponsored by Uniformed Services University of the Health Sciences and is currently Not yet recruiting. The study focuses on Contraception. Target enrollment is 120 participants.
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Study Focus
Sponsor & Location
Uniformed Services University of the Health Sciences
Timeline & Enrollment
Phase 4
Jun 01, 2023
Jan 01, 2024
Primary Outcome
Procedure time,Patient-reported pain level
Summary
The goal of this clinical trial is to perform a pilot study looking at the benefit of topical
 anesthetic application to the cervix by tampon prior to intra-uterine device insertion. The
 main question it aims to answer are:
 
 - Does patient tampon-applied local anesthetic prior to insertion of an intrauterine
 device (IUD) reduce procedural duration?
 
 - Does patient tampon-applied local anesthetic prior to insertion of an intrauterine
 device (IUD) reduce pain and improve patient perceptions of the procedure? Participants
 will place a tampon after dipping the tampon into the study-supplied medication (aqueous
 lidocaine or saline). Researchers will compare treatment and control groups to see if
 there is any difference in procedure time, difficulty or patient perceptions.
ICD-10 Classifications
Data Source
ClinicalTrials.gov
NCT05890495
Non-Device Trial