Can a warmer fluid make a gynecologic procedure less painful?
NCT ID NCT07773376
First seen Aug 19, 2026 · Last updated Aug 20, 2026 · Updated 1 time
Summary
This trial asks whether using saline warmed to body temperature (37°C) during outpatient hysteroscopy—a procedure to look inside the uterus—can reduce pain compared with saline at room temperature. Women aged 18 to 70 scheduled for diagnostic hysteroscopy will be randomly assigned to receive either warm or room-temperature saline. Pain scores will be compared during the procedure and one hour later, along with the need for extra pain relief. The hope is that a simple temperature change could make the experience more comfortable.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Warmed saline at 37°C used as a uterine distension medium during hysteroscopy
- What this could lead to
- If warm saline works, it could offer a simple, low-cost way to make outpatient hysteroscopy more comfortable and reduce the need for pain medication.
- What could go wrong
- This is a small, early-stage trial, and the benefit may be modest or not clearly better than room-temperature saline. Pain is subjective, and results may not apply to all women.
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 60 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2026
An estimate. Start dates often move.
- Expected to finish
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Dec 2026
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 to 70 years
- Sex
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Female participants only
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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: * Age 18-70 years. * Ability to understand and report pain using the Visual Analog Scale. * Willingness to undergo outpatient hysteroscopy and provide written informed consent. Exclusion Criteria: * Congenital genital tract malformations: including these patients could introduce a confounding factor because pain may result from difficult anatomy rather than the temperature of the distension medium. * Previous hysteroscopic procedures: pain perception may be influenced by prior experience rather than the intervention itself * Suspected pregnancy: standard gynecologic practice considers pregnancy a contraindication to elective diagnostic hysteroscopy * Active pelvic infection: instrumentation of an infected genital tract may increase morbidity and facilitate ascending infection. Also, pain scores may reflect infection-related pain rather than procedural pain.
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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
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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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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Ain Shams University Maternity Hospital
Cairo, Egypt
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