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Which method is safer for pregnancy termination in scarred uterus?

NCT ID NCT07604051

Disease control Sponsor: Dr Mudassar Saeed Pansota 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study looked at 60 women with a scarred uterus who needed to end a pregnancy in the second trimester. It compared two methods: a medicine called PGE1 and a balloon device called a cervical Folley. The goal was to see which one works better and causes fewer problems.

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

Phase 4

Runs after approval, following long-term safety and how well the treatment works in everyday use.

Participants

60 people

The number who actually took part.

Started

Nov 2025

Finished

May 2026

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.

Ages

20 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: * All women presented for termination of pregnancy (as per-operational definition). * Patients with age 20-45 years Exclusion Criteria: * Women having multiple gestation. * Women having any complication of miscarriage like bleeding, chorioamnionitis, disseminated intravascular coagulopathy. * Women having any complication in previous cesarean like endometritis, re opening and scar dehiscence. * Patients with molar or ectopic pregnancy (assessed on ultrasonography).

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As listed by the trial registrant

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

Termination of pregnancy

Contacts and locations

Locations

  • Hilal-e-ahmar Hospital

    Faisalabad, Punjab Province, 60000, Pakistan

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