Red flag system aims to prevent fainting during office hysteroscopy
NCT ID NCT07030218
First seen Jun 30, 2026 · Last updated Jul 01, 2026 · Updated 1 time
Summary
This study tests a new 'red flag' classification system to predict which women might faint or feel faint during office hysteroscopy, a procedure where a small camera is inserted into the uterus. Researchers will monitor 100 women for signs of distress and pain during the procedure, comparing their experience to normal menstrual pain. The goal is to see if this simple checklist can help doctors improve safety and comfort for future patients.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could lead to a simple checklist that helps doctors identify women at risk of fainting during hysteroscopy, making the procedure safer.
- What could go wrong
- This is a small pilot study with only 100 participants, so the red flag system may not work as well in larger, more diverse groups. It is designed to test feasibility, not to prove effectiveness.
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.
- 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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Jun 2025
- Expected to finish
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Jul 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.
Who is studied
women undergoing office hysteroscopy in the hospital / outpatient
- Ages
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18 years and older
- 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: * Women ≥18 years * Prior gynecological care * Informed consent provided Exclusion Criteria: * Inability to consent * Psychiatric disorders or anxiolytic use * Use of dilators or anesthesia above level 3a * Family history of VVS
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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.
Contacts and locations
Locations
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Tanvir Hospital
Hyderabad, Telangana, 500073, India
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Other studies related to the condition(s) this trial covers.