AzTrials
AzTrials

LabourRCT NICE ACOGNCT07764406

Effect Of Amniotomy In Early Labour On Duration Of Labour

A study testing Amniotomy (intentional rupture of amniotic sac during labour) in people with Labour, run by Indus Hospital and Health Network at 1 site in Pakistan.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
Search all trials

Trial summary

The goal of this clinical trial is to learn if intentional rupturing of amniotic sac in early labour works to shorten the duration of labour. The main question it aims to answer is . Read more about this study

Who is it for?
Ages 18 to 45 years, women only
Conditions the study is for
Labour
What is being tested?
Amniotomy (intentional rupture of amniotic sac during labour)
Type of treatment
Surgery or procedure
Could I receive a placebo?
No, everyone receives an active treatment
How many people
60 participants
Where
1 sitePakistan
Study dates
1 Oct 2025to 28 Apr 2026
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 45 years
  • Women only
  • No healthy volunteers
  • Adult

Who may be able to join

  • 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)

Who cannot join

  • 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)

Trial locations and contacts

1 site in 1 country.

Pakistan1 site
  • Indus hospital and health network

    Multan, Punjab Province, 34200

Other trials in Pakistan

About this study

Official title: Effect Of Amniotomy In Early Labour On Duration Of Labour In Primigravida At Term Pregnancy: A Randomized Controlled Trial

The goal of this clinical trial is to learn if intentional rupturing of amniotic sac in early labour works to shorten the duration of labour.

The main question it aims to answer is

Read more

. Does the intentional rupture of amniotic sac in early labour lowers the duration of labour in primigravida at term as compared to expectant management.

The researchers will compare mean duration of labor in intentional rupture of amniotic sac in early labour group to expectant management untill spontaneous rupture of amniotic sac in primigravida at term pregnancy.

The participants will be randomly assigned to group A and B through lottery method using sealed opaque envelopes.

In group A, amniotomy at 3cm will be done using aseptic measurements with the help of forcep. while in group B, membranes will be left intact. A partograph will be maintained in all patients throughout labor. Duration of each stage of labour will be monitored as per operational definition by the nurse not aware of treatment given. Fetal and maternal monitoring will be done half hourly till delivery of infant. Cesarean-section will be done in non-reactive CTG patients. In case of any of the adverse events related to intervention like placental abruption and cord prolapse [that is less likely as the subjects are primigravida patients in which head is mostly already engaged before onset of labour], and presence of meconium upon ARM that is not related to intervention individualized care will be provided like continuous electronic fetal monitoring and emergency caserean section will be kept in hand. If any adverse event occur related to intervention it will be reported to IRB within 24hours. All the patients will be kept under observation for 24 hours after delivery. All the data will be recorded on proforma

Read the detailed description

Effect of Amniotomy in Early Labour on Duration of Labour in Primigravida at Term Pregnancy: A Randomized Controlled Trial.

Introduction Labor is a physiological but painful experience for women. It is a dynamic and ongoing process that culminates with the delivery of a healthy baby, followed by the ejection of the placenta and membranes.After active labor has begun, the membranes burst, which is known as spontaneous membrane rupture.Amniotomy is the artificial breach of the amniotic membrane with the primary goal of accelerating contraction and shortening the duration of labor.Studies have shown that amniotomy procedure is very effective to reduce the time duration of labour and maternal risk factors. Amniotomy method is also applied when internal monitoring of fetus is required.

The mechanism of action behind amniotomy is thought to be the release of prostaglandin E2 (PGE2) and rise of oxytocin level.Routine early amniotomy appears to be associated with both benefits and risks. It's typically used to accelerate labour and was originally thought to decrease caesarean section rates. Amniotomy is a frequent and low-cost method of inducing labor. The link between early amniotomy and severe maternal morbidity varied according to maternal factors, while early amniotomy was not linked to newborn morbidity.

The current study has been planned to examine the effect of amniotomy in terms of reducing the time duration of labour in primigravida at term gestation. The study results obtained from our local setting will be useful for expertise while selecting the mode of delivery. Evidence-based guidelines will help in practicing standardize care, reduce variability in practice, reduce maternal and neonatal mortality and improve overall outcomes for mothers and babies.

Objective: To compare mean duration of labor in amniotomy compared to spontaneous rupture of membrane in primigravida at term pregnancy.

Operational definitions

Duration of labour: Time (hours) during active labour encompassing 1st and 2nd stage of labour will be noted using a stopwatch by nurse on duty. 1st stage will be labelled from cervical dilatation of 3-4 cm in active labor to full dilatation of cervix (≈ 10 cm) by vaginal examination conducted every 2 hours. The 2nd stage of labour will consist of a phase of active labour from full dilatation to delivery.

Body mass index (BMI): BMI will be calculated by formula- weight in kg/height in meter2. Weight will be measured on a weighing scale and height on stadiometer.

Hypothesis: Mean duration of labour is lower in amniotomy group compared to spontaneous rupture of membrane.

Material \& methods

Setting: Department of OBG, Recep Tayyip Erdoğan Hospital, Muzaffargarh

Study design: Randomized Controlled Trial

Duration: 6-months after approval of synopsis

Sample size10: Sample size is calculated through OpenEpi software using formula for mean difference. Where,

Labour duration in amniotomy group = 5.725±0.59 hours Power of the study = 80%

Labour duration in spontaneous membrane rupture = 7.150±0.48 hours

Confidence level = 95% Sample size = 60 (30 in each group)

Sampling technique: Non-probability consecutive sampling

Data collection procedure

Prior approval will be sought from the ethics review committee. A total of 60 women in labour room with active labour, fulfilling the inclusion criteria, will be enrolled with volountry participation after informed consent and confidentiality will be maintained. Baseline characteristics including age, body mass index and gestational age (by LMP method) will be recorded from all the participants. The participants will be randomly assigned to group A and B through lottery method using sealed opaque envelopes.

In group A, amniotomy at 3cm will be done using aseptic measurements with the help of

Kocher's forceps while in group B, membranes will be left intact. A partograph will be maintained in all patients throughout labor. Duration of each stage of labour will be monitored as per operational definition by the nurse not aware of treatment given. Fetal and maternal monitoring will be done half hourly till delivery of infant. Cesarean-section will be done in non-reactive CTG patients. In case of any of the adverse events related to intervention like placental abruption and cord prolapse [that is less likely as the subjects are primigravida patients in which head is mostly already engaged before onset of labour], and presence of meconium upon ARM that is not related to intervention individualized care will be provided like continuous electronic fetal monitoring and emergency caserean section will be kept in hand. If any adverse event occur related to intervention it will be reported to IRB within 24hours. All the patients will be kept under observation for 24 hours after delivery. All the data will be recorded on proforma

Data analysis The data will be analysed through SPSS version 23. The normality of numerical data will be assessed through the Shapiro-Wilk test. Age, BMI, gestational age and duration of labour will be presented as mean and standard deviation. Duration of labour will be compared between group A and group B through independent sample t-test and p-value ≤ 0.05 will be taken as significant. The data will be stratified on age groups, gestational age and BMI categories to determine the effect on duration of labour between group A and B. Post-stratification independent sample t-test will be applied and p-value ≤ 0.05 will be taken as significant.

Conditions
Labour
Being tested
Amniotomy (intentional rupture of amniotic sac during labour)
Keywords
Amniotomy in early labour, Effect of amniotimy in early labour in primigravida at term

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Amniotomy (intentional rupture of amniotic sac during labour)Procedure or surgery

    intentional rupture of amniotic sac during labour)

Study groups in NCT07764406
Study groupRoleWhat they receive
Group A-Amniotimy groupActive comparatoramniotomy performed at 3 cm cervical dilatation using aseptic technique
Receives: Procedure: Amniotomy (intentional rupture of amniotic sac during labour)
Group B-Expectant groupNo interventionMembranes left intact untill spontaneous rupture of membranes occur

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Mean duration of labour in amniotomy group and spontaneous rupture of membranes in primigravida at term pregnancy

    To compare the mean duration of labour in primigravida at term pregnancy undergoing amniotomy in early labour at 3-4 cm cervical dilatation versus expectant management until spontaneous rupture of membranes.

    Measured: 6 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted13 Aug 2026
  2. Study start1 Oct 2025
  3. Primary completion30 Mar 2026
  4. Study completion28 Apr 2026

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
Study design: Randomized Controlled Trial Duration: 6-months after approval of synopsis Sample size: Sample size is calculated through OpenEpi software using formula for mean difference. Where, Labour duration in amniotomy group = 5.725±0.59 hours Power of the study = 80% Labour duration in spontaneous membrane rupture = 7.150±0.48 hours Confidence level = 95% Sample size = 60 (30 in each group) Sampling technique: Non-probability consecutive sampling The participants randomly assigned to group A and B through lottery method using sealed opaque envelopes
Masking
None (open label)
Enrolment
60 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07764406
Sponsor's protocol ID
IHHN_IRB_2025_05_019
Acronym
RCT NICE ACOG
Status last verified
Jul 2026
First submitted
6 Jul 2026
Last updated
13 Aug 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

A study testing Amniotomy (intentional rupture of amniotic sac during labour) in people with Labour, run by Indus Hospital and Health Network at 1 site in Pakistan.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 13 Aug 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Pakistan. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Mean duration of labour in amniotomy group and spontaneous rupture of membranes in primigravida at term pregnancy (time frame: 6 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 13 Aug 2026.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in