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Uterine scar tissue after fibroid surgery: who is at risk?

NCT ID NCT04030273

Knowledge-focused Sponsor: Università degli Studi dell'Insubria Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

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
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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Aug 12, 2026 · Last updated Aug 18, 2026 · Updated 3 times

Summary

This study looks at how often women develop intrauterine adhesions (scar tissue inside the uterus) after having fibroids removed through laparoscopic or open surgery. Researchers will check for adhesions using a small camera inserted into the uterus three months after surgery. They will also track medical and surgical details to see which factors are linked to a higher chance of developing these adhesions.

What this could mean

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

Active substance
Diagnostic hysteroscopy (a camera look inside the uterus)
What this could lead to
If it works, this could help identify which women are more likely to develop uterine scar tissue after fibroid surgery, guiding closer follow-up or preventive care.
What could go wrong
This is a small observational study, so it can only show associations, not cause and effect. Results may not apply to all women or all surgical techniques.

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

62 people

The number who actually took part.

Started

Jan 2020

Finished

Mar 2021

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.

Who is studied

Female patients from 18 to 45 years of age with the diagnosis of uterine fibroids, wish to preserve fertility/uterus, not candidates for hysteroscopic myomectomy, who underwent laparoscopic or laparotomic myomectomy were considered eligible.

Ages

18 to 45 years

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: * Diagnosis of one or more uterine myomas * Desire to preserve fertility/uterus * Myomectomy (by laparotomy or laparoscopy) Exclusion Criteria: * Adults unable to consent * Pregnant women * Prisoners * History of previous intrauterine procedures such as dilation and curettage * History of known intrauterine adhesions * History of documented pelvic inflammatory disease * History of endometritis (acute or chronic) * Hysteroscopic myomectomy

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Conditions

The condition(s) this trial relates to.

gynatresia leiomyoma myofibroma uterine corpus leiomyoma

As listed by the trial registrant

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

Myoma;uterus

Contacts and locations

Locations

  • Ospedale "Filippo Del Ponte"

    Varese, Italy

More trials for these conditions

Other studies related to the condition(s) this trial covers.