Amniotomy and Oxytocin for Augmentation of Labour
AOAL
Concurrent Versus Sequential Administration of Amniotomy and Oxytocin for Augmentation of Labour: a Randomized Controlled Trial
1 other identifier
interventional
150
0 countries
N/A
Brief Summary
Prolonged labour is a cause of maternal mortality and morbidity and perinatal mortality and morbidity. Prolonged labour is most often defined as onset of regular , rhythmical painful contractions accompanied by cervical dilatation where labour is longer than 24 hours.prolonged active phase should not last longer than 12 hours without full assessment in a facility able to offer management and treatment of complications.Causes of prolonged labour usually due to poor or uncoordinated uterine action , fetal head malposition , and or abnormal pelvis either due to bone or soft tissue obstruction. Arrested or prolonged labor is a frequent indication of cesarean delivery.Prolonged labor is also associated with increased pain and negative birth experience. Women with a prolonged first stage of labor have experienced a higher rate of postpartum hemorrhage, chorioamnionitis and neonatal admission to the intensive care unit. Caesarean section rates are over 20% in many developed countries and have increased nearly four-fold relative to the 5% rate observed in the early 1970s. The main diagnosis contributing to this increase is dystocia or prolonged labor.Data obtained from local hospital records showed that Caesarean section rate in Assiut University Women's Health Hospital is 47.96% at 2013. Dystocia is a term used for delay of labor progress and usually refers to abnormally slow cervical dilatation.It has been proposed that the partogram should include, as a diagnostic criterion, a 1 cm/hour line originating at admission. The World Health Organization has proposed a modified partogram that recommends that active phase be diagnosed only at 4 cm or more. Oxytocin augmentation of uterine contractions with or without amniotomy is widely used in the modern obstetric practice to treat a slow labour, although the timing of oxytocin initiation and amniotomy may vary widely.This intervention is based on the hypothesis that the most frequent cause of dystocia is inadequate uterine contraction. The mechanism by which amniotomy speeds up labour remains unclear it is thought that when the membranes are ruptured ,the production and release of prostaglandins and oxytocin increases resulting in stronger contractions and quicker cervical dilatation. I has been found that early intervention (augmentation versus routine care ) with amniotomy and oxytocin to be associated with a modest reduction in the risk of caesarean section. Moreover, amniotomy found to be associated with an increased risk of cesarean delivery compared with women without amniotomy for shortening of spontaneous labour. The 3 methods ( Amniotomy, Oxytocin or both) used for augmentation of labor in different settings without a real conclusion which is better.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for phase_2
Started Apr 2014
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
April 1, 2014
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 1, 2014
CompletedFirst Submitted
Initial submission to the registry
October 5, 2014
CompletedFirst Posted
Study publicly available on registry
December 17, 2014
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2015
CompletedNovember 21, 2017
November 1, 2017
5 months
October 5, 2014
November 20, 2017
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Rate of cervical dilatation
The rate of cervical dilation cm/ hour
every hour up to full cervical dilatation
Secondary Outcomes (2)
Augmentation delivery time
Time ( in minutes) between the start of augmentation of labor up to the delivery of the head
Apgar score at 10 minutes
from 0-10 minutes
Study Arms (3)
Amniotomy first
ACTIVE COMPARATORWill be done with sterile gloves after insurance that is the baby's head fits in the pelvis ( 3\\5 or less of fetal head felt by first pelvic grip ) and by vaginal examination the head at station zero . The membranes are then punctured using an a hook during uterine contractions.
Oxytocin first
ACTIVE COMPARATORThe starting dose will be the low dose rate equal or less than 4 m unit\\minute (4 drops\\minute doubled every 15 minutes up to 40 drops \\minute) as intravenous drip on dextrose ,Ringer's lactate or saline solution.
Amniotomy and oxytocin
ACTIVE COMPARATORAmniotomy will be done (as explained above) and oxytocin (the same regimen mentioned above) at the same time.
Interventions
Rupture of membranes and administration of oxytocin to augment labor
Eligibility Criteria
You may qualify if:
- Women in spontaneous labor
- Women with intact membranes at the time of randomization
- Single fetus
- Vertex presentation
- Cervical dilatation 3 cm or more
- Gestational age 37 weeks or more proved by reliable dates or by early ultrasound scan in the first trimester
- Slow progress in the active phase of labor ( cervical dilatation less than 1 cm \\hour)
You may not qualify if:
- Women with a previous uterine scar
- Severe preeclamptic toxemia
- Suspected fetal macrosomia (greater than 4000 g)
- Women with any congenital malformations
- Women with Intra uterine fetal death
- Diabetes mellitus with pregnancy
- Antepartum hemorrhage
- Women with other indications of caesarean section
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- phase 2
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Dr.
Study Record Dates
First Submitted
October 5, 2014
First Posted
December 17, 2014
Study Start
April 1, 2014
Primary Completion
September 1, 2014
Study Completion
December 1, 2015
Last Updated
November 21, 2017
Record last verified: 2017-11