Can a simple drape ease the discomfort of gynecologic exams?

NCT ID NCT07797309

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only This study
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Sep 01, 2026 · Last updated Sep 02, 2026 · Updated 1 time

Summary

This trial tests whether a specially designed drape that covers a woman's lower body during a vaginal exam can reduce pain and improve satisfaction and perceived privacy. Women aged 18 and older undergoing a vaginal exam at a gynecology clinic are randomly assigned to use the drape or receive the clinic's usual care. Right after the exam, they rate their pain, satisfaction, and sense of privacy. The goal is to see if this simple change makes the experience more comfortable and dignified.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
A specially designed drape that covers the lower body during vaginal examination, exposing only the area being examined.
What this could lead to
If effective, this drape could become a simple, low-cost way to improve comfort and dignity for women during routine gynecologic exams.
What could go wrong
The trial is small and early, and the drape may not meaningfully change pain or satisfaction. Results depend on how women perceive the drape, which can vary widely.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 100 people

The number the study aims to enrol. It can still change while the study runs.

Started

Aug 2026

Expected to finish

Feb 2027

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 years and older

Sex

Female participants only

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Aged 18 years or older * Undergoing vaginal examination Exclusion Criteria: * Clinical condition requiring emergency obstetric or gynaecological intervention * A health problem preventing cognition or communication * Diagnosed psychological disorder (depression, post-traumatic stress disorder, bipolar disorder)

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Conditions

The condition(s) this trial relates to.

Pain Patient Satisfaction

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    The full official record for this study. This one lists no contact details, but it is the first place any would appear.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Osmaniye Training and Research Hospital, Gynaecology and Obstetrics Clinic

    Osmaniye, Turkey (Türkiye)

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