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.
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
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 group | Role | What they receive |
|---|---|---|
| Group A-Amniotimy group | Active comparator | amniotomy performed at 3 cm cervical dilatation using aseptic technique Receives: Procedure: Amniotomy (intentional rupture of amniotic sac during labour) |
| Group B-Expectant group | No intervention | Membranes 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.
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.
- First posted13 Aug 2026
- Study start1 Oct 2025
- Primary completion30 Mar 2026
- Study completion28 Apr 2026
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for LabourStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Indus Hospital and Health Network
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Bushra Iqbal, Indus Hospital and Health Network
- Investigators
- Bushra Iqbal, MBBS, Principal investigator, Indus Hospital and Health Network
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
Study at a glance
From the registry record, last updated by the sponsor on 13 Aug 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Effect Of Amniotomy In Early Labour On Duration Of Labour In Primigravida At Term Pregnancy: A Randomized Controlled Trial
- ClinicalTrials.gov ID
- NCT07764406
- Acronym / sponsor ID
- RCT NICE ACOG / IHHN_IRB_2025_05_019
- Conditions
- Labour
- Keywords
- Amniotomy in early labour, Effect of amniotimy in early labour in primigravida at term
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 60 participants (actual)
- Lead sponsor
- Indus Hospital and Health NetworkUniversity, hospital or other
- Study start
- 1 Oct 2025 (actual)
- Primary completion
- 30 Mar 2026 (actual)
- Study completion
- 28 Apr 2026 (actual)
- First posted
- 13 Aug 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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
. 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
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.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
- 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
| Arm | Type | Receives |
|---|---|---|
| Group A-Amniotimy group | Active comparator | Procedure: Amniotomy (intentional rupture of amniotic sac during labour)amniotomy performed at 3 cm cervical dilatation using aseptic technique |
| Group B-Expectant group | No intervention | –Membranes left intact untill spontaneous rupture of membranes occur |
Who may qualify
- Ages
- 18 to 45 years
- Sex
- Female only
- Healthy volunteers
- Not accepted
- Age groups
- Adult
Key inclusion criteria (4 listed)
- 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)
Key exclusion criteria (3 listed)
- 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)
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Amniotomy (intentional rupture of amniotic sac during labour)intentional rupture of amniotic sac during labour) | Procedure or surgery | Group A-Amniotimy group |
Primary outcome
Mean duration of labour in amniotomy group and spontaneous rupture of membranes in primigravida at term pregnancy
Time frame: 6 months
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.
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 13 Aug 2026.
- Related InfoLink provided by the sponsor.
- Related InfoLink provided by the sponsor.
- Related InfoLink provided by the sponsor.
- Related InfoLink provided by the sponsor.
- Related InfoLink provided by the sponsor.
- Related InfoLink provided by the sponsor.
- Individual participant dataSharing planned: Undecided
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Bushra Iqbal, MBBS principal investigator
Indus Hospital and Health Network
1 site in 1 country: see every site and its status.
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.