Can a glowing dye reveal a Woman's fertility after ovarian cyst surgery?
NCT ID NCT04355312
First seen Aug 07, 2026 · Last updated Aug 07, 2026
Summary
This trial tests whether a green dye, injected during keyhole surgery to remove benign ovarian cysts, can show how well the ovary is still getting blood flow. The idea is that better blood flow might mean the ovary is healthier and more likely to support a future pregnancy. Women under 42 who want to conceive soon and are having a cyst removed will be enrolled. The dye's glow is compared with standard tests of ovarian reserve over the next year to see if it could be a quick, reliable indicator of fertility potential.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Indocyanine green dye injected during laparoscopic ovarian cystectomy to assess blood flow to the ovary
- What this could lead to
- If it works, this could give women a quick, real-time read on their ovarian health after cyst removal, helping them make faster decisions about fertility treatment or egg freezing.
- What could go wrong
- This is a small feasibility study, so the dye's ability to predict fertility is unproven. The dye may not reliably reflect ovarian reserve, and there are rare risks of allergic reactions to the dye.
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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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51 people
The number who actually took part.
- Started
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Jun 2020
- Finished
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Dec 2022
- 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 42 years
- 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: * An adult woman of childbearing potential who has a desire for short-term pregnancy, under the age of 42, to undergo laparoscopic accessible surgical treatment (\<10 cm) for a benign organic ovarian cyst (serous, mucinous, dermoid or endometriotic) whose diagnosis was made on imaging (ultrasound or MRI). * Patient able to provide informed consent to her participation in the study. * Patient covered by the " Sécurité Social " insurance system. Exclusion Criteria: * Adult patient under protection, tutorship or curatorship. * Refusal of the patient or poor understanding of the French language. * Known allergy to iodine. * Current pregnancy or breastfeeding
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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
-
CHU de Clermont-Ferrand
Clermont-Ferrand, 63000, France
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