RecruitingNot ApplicableNCT05458037

RCT of Pain Perception With Fast and Slow Tenaculum Application

A Randomized Controlled Trial of Pain Perception With Fast and Slow Tenaculum Application to the Uterine Cervix


Sponsor

Women and Infants Hospital of Rhode Island

Enrollment

150 participants

Start Date

Sep 29, 2020

Study Type

INTERVENTIONAL

Conditions

Summary

This project will be a randomized controlled trial (RCT) measuring pain perception with two different tenaculum placement techniques on the uterine cervix. A tenaculum is an instrument used to hold the cervix (the opening to the uterus or womb) in place. The trial will measure pain perception with a Visual Analog Scale (VAS) from 0 to 100 mm for two different tenaculum placement techniques, fast and slow closure on the uterine cervix. The main objective of this study is to determine if there is a difference in pain perception with fast compared to slow tenaculum placement techniques on the uterine cervix. We hypothesize that the slow technique will be perceived as less painful for subjects as measured on a 0 mm to 100 mm Visual Analog Scale (VAS). Subsidiary objectives include describing overall pain levels during the procedure.


Eligibility

Sex: FEMALEMin Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a procedure called Speed of tenaculum application for people with pain, acute and pain, procedural. The study is currently recruiting participants at 1 location. People eligible for this study include women aged 18 Years and older.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

PROCEDURESpeed of tenaculum application

Fast or slow closure of the tenaculum for application to the uterine cervix


Locations(1)

Women and Infants Hospital

Providence, Rhode Island, United States

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NCT05458037


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