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Could breaking the water early speed up labour?

NCT ID NCT07764406

What the study statuses mean

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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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 13, 2026 · Last updated Aug 14, 2026 · Updated 1 time

Summary

This trial tests whether intentionally rupturing the amniotic sac (breaking the water) early in labour shortens the overall duration of labour in first-time mothers with a full-term pregnancy. Participants are randomly assigned to either have the procedure at 3 cm dilation or to wait for the sac to break naturally. Researchers will compare the average length of labour between the two groups, while closely monitoring both mother and baby for safety.

What this could mean

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

Active substance
Amniotomy (intentional rupture of the amniotic sac during labour)
What this could lead to
If effective, this simple procedure could shorten labour for first-time mothers, potentially reducing distress and the need for further interventions.
What could go wrong
This is a small early-stage trial, and results may not apply to all women. Risks include placental abruption, cord prolapse, and infection, though these are considered less likely in this population.

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

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

60 people

The number who actually took part.

Started

Oct 2025

Finished

Apr 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

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: * Age 18 - 45 years * Primigravida, singleton fetus (on antenatal scan) * Full term - gestational age 37 - 41 weeks * Established labour (presence of regular uterine contractions - 3 per 10 minutes) Exclusion Criteria: * History of chronic hypertension, diabetes mellitus, gestational diabetes - on medical record * Rupture of the membrane (pooling of fluid in vaginal on speculum examination) * History of antepartum hemorrhage (history and medical record)

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As listed by the trial registrant

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

Contacts and locations

Locations

  • Indus hospital and health network

    Multan, Punjab Province, 34200, Pakistan

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