Clinical Trials Logo

Clinical Trial Summary

Women will be admitted when active phase of labour starts defined as the presence of at least three regular uterine contractions over 10 minutes with cervical dilatation four centimeters with cervical effacement not less than 50% and no progress of labor for 2 hours or more. Amniotomy was done in those with intact membrane and continuous electronic fetal monitoring was done. Women with prolonged labor after these measures were randomly divided using automated web-based randomization system into 2 equal groups. Group I included 50 women received 40mg HBB (Buscopan, Memphis Co, Giza, Egypt) intravenous bolus injection. Group II included 50 women received 2 ml of normal saline. The obstetrician, participants and outcome assessor were all blinded to the group assignment. Labor will be monitored by Vaginal examination every two hours. The duration of the first stage was calculated from the time of cervical dilatation of three to four centimeters in active labor until a fully dilated cervix was observed.


Clinical Trial Description

Women will be admitted when active phase of labour starts defined as the presence of at least three regular uterine contractions over 10 minutes with cervical dilatation four centimeters with cervical effacement not less than 50% and no progress of labor for 2 hours or more. Amniotomy was done in those with intact membrane and continuous electronic fetal monitoring was done. Women with prolonged labor after these measures were randomly divided using automated web-based randomization system into 2 equal groups. Group I included 50 women received 40mg HBB (Buscopan, Memphis Co, Giza, Egypt) intravenous bolus injection. Group II included 50 women received 2 ml of normal saline. The obstetrician, participants and outcome assessor were all blinded to the group assignment. Labor will be monitored by Vaginal examination every two hours. The duration of the first stage was calculated from the time of cervical dilatation of three to four centimeters in active labor until a fully dilated cervix was observed. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03430362
Study type Interventional
Source Cairo University
Contact
Status Completed
Phase N/A
Start date March 2, 2018
Completion date February 16, 2020

See also
  Status Clinical Trial Phase
Completed NCT01402310 - Bishop Score, Cervical Length and Multiple Proteins in Cervicovaginal Fluid at 40 Weeks to Predict Onset of Labor N/A
Completed NCT00915148 - Ultrasound Prediction of Prolonged Labour N/A
Completed NCT02334150 - Epidural Analgesia on Electrophysiological Function Phase 2/Phase 3
Recruiting NCT05489315 - Quantifying the Impact of the Peanut Ball on the Duration of the Active Stage of Labor N/A
Completed NCT05206409 - Prediction of Delivery Mode by Ultrasound-assessed Fetal Position in Nulliparous Women With Prolonged First Stage of Labor.
Recruiting NCT01854073 - Hyoscine Butyl Bromide for Management of Prolonged Labor Phase 3
Recruiting NCT06268431 - Oxytocin Rest to Reduce Cesarean Delivery N/A
Completed NCT03509103 - Electronic Partograph: A Way of Improving Partograph Use During Labour Monitoring Process in Selected District Hospitals in Bangladesh N/A
Completed NCT02318121 - Amniotomy and Oxytocin for Augmentation of Labour Phase 2