Can a simple drape ease the discomfort of gynecologic exams?
NCT ID NCT07797309
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
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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
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About 100 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Aug 2026
- Expected to finish
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Feb 2027
An estimate. End dates often move.
- Lead sponsor
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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
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18 years and older
- Sex
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Female participants only
- Healthy volunteers
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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 Hide 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.
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.
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The places running it
1 site. The list below names each one and where it is.
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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.
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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
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Osmaniye Training and Research Hospital, Gynaecology and Obstetrics Clinic
Osmaniye, Turkey (Türkiye)
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