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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT04216628
Other study ID # 31-19-AAA
Secondary ID
Status Terminated
Phase N/A
First received
Last updated
Start date February 10, 2020
Est. completion date January 11, 2023

Study information

Verified date August 2023
Source Assuta Ashdod Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The objective of this study is to investigate the course of labor in early versus late amniotomy following balloon cervical ripening in women undergoing term induction of labor stratified by parity.


Description:

Induction of labor is a common obstetric procedure with a reported rate of 23.3% in 2012 in the United State. It has been recently reported that Induction of labor at full term in uncomplicated singleton gestations is not associated with increased risk of cesarean delivery and overall has similar outcomes compared to expectant management. Induction of labor in women with an unripened cervix is comprised of two stages, cervical ripening followed by augmentation of labor. Extra amniotic balloon inflation is a widespread mechanical method of cervical ripening that commonly results in a ripened cervix open to 3-4 cm without significant uterine contractions. At this point the clinician may opt to perform artificial rupture of membranes or rather first begin oxytocin infusion delaying amniotomy to later stages of labor. A retrospective cohort showed early amniotomy after Foley balloon catheter removal was associated with shorter duration of labor induction among nulliparous women.In accordance, an RCT investigating the efficacy of early amniotomy in nulliparous women showed this practice resulted in labor shortening without increasing the rate of cesarean section, yet these women were treated by different methods for cervical ripening. Contradicting results were shown in a randomized controlled trial addressing the very question of early versus late amoniotomy after balloon ripening, concluding that postponing amniotomy until active labor commences results in a reduction of dystocia indicated cesarean section. However no distinction was made in this study between nulliparous and multiparous parturients. Since these comprise different groups with distinct labor curves, the question remains whether one should consider parity when deciding to perform early vs late amniotomy following balloon expulsion. Both Amniotomy and Oxytocine infusion are part of the routine protocol and necessary procedures for induction of labor. Adverse outcome of amniotomy includes fetal heart rate changes, cord prolapse and intrapartum fever when labor is prolonged. Adverse outcome of oxytocine include hypertonus and fetal heart rate changes requiring cessation of oxytocine infusion (as in routine protocol) and intrapartum fever if labor is prolonged (not due to oxytocine infusion per se). Most of the patients admitted for induction of labor will need both amniotomy and oxytocine, however the role of the order of these two procedures is unclear ,as well as whether the order of these procedures affect the rate of adverse outcome. The objective of this study is to investigate the course of labor in early versus late amniotomy following balloon cervical ripening in women undergoing term induction of labor stratified by parity. STUDY PROTOCOL Multicenter randomized control trial that will be conducted in 4 medical centers in Israel. Women with a singleton viable gestation undergoing indicated labor induction at term (37-42 weeks of gestation) who undergoing induction of labor at term with a low bishop score<4 who require extra amniotic balloon cervical ripening will be asked to participate in the study. Written informed consent will be obtained from all patients. Early amniotomy- Amniotomy performed as the exclusive primary intervention to augment labor following expulsion of the EAB regardless of cervical dilatation. Late amniotomy- EAB expulsion is followed by oxytocin infusion at increasing increments as the primary intervention as an exclusive intervention for at least 2 hours.


Recruitment information / eligibility

Status Terminated
Enrollment 146
Est. completion date January 11, 2023
Est. primary completion date January 11, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria: 1. Gestational age 37-42 weeks 2. Singleton pregnancy 3. Vertex presentation 4. Medical indication for induction of labor 5. Need for cervical ripening (Bishop score <=6) 6. Consent to participate in the study 7. Women age at or >18 years Exclusion Criteria: 1. Multiple pregnancies 2. Preterm pregnancy 3. Previous cesarean section 4. Uterine malformation 5. Withdrawal of consent.

Study Design


Related Conditions & MeSH terms

  • Induction of Labor Affected Fetus / Newborn

Intervention

Other:
Amniotomy
Artificial rupturing of membranes and IV infusion of Oxytocin

Locations

Country Name City State
Israel Assuta Ashdod Ashdod

Sponsors (4)

Lead Sponsor Collaborator
Assuta Ashdod Hospital Rambam Health Care Campus, The Baruch Padeh Medical Center, Poriya, Wolfson Medical Center

Country where clinical trial is conducted

Israel, 

References & Publications (9)

ACOG Practice Bulletin No. 107: Induction of labor. Obstet Gynecol. 2009 Aug;114(2 Pt 1):386-397. doi: 10.1097/AOG.0b013e3181b48ef5. No abstract available. — View Citation

Battarbee AN, Palatnik A, Peress DA, Grobman WA. Association of Early Amniotomy After Foley Balloon Catheter Ripening and Duration of Nulliparous Labor Induction. Obstet Gynecol. 2016 Sep;128(3):592-597. doi: 10.1097/AOG.0000000000001563. — View Citation

Jozwiak M, Bloemenkamp KW, Kelly AJ, Mol BW, Irion O, Boulvain M. Mechanical methods for induction of labour. Cochrane Database Syst Rev. 2012 Mar 14;(3):CD001233. doi: 10.1002/14651858.CD001233.pub2. — View Citation

Levy R, Ferber A, Ben-Arie A, Paz B, Hazan Y, Blickstein I, Hagay ZJ. A randomised comparison of early versus late amniotomy following cervical ripening with a Foley catheter. BJOG. 2002 Feb;109(2):168-72. doi: 10.1111/j.1471-0528.2002.01137.x. — View Citation

Macones GA, Cahill A, Stamilio DM, Odibo AO. The efficacy of early amniotomy in nulliparous labor induction: a randomized controlled trial. Am J Obstet Gynecol. 2012 Nov;207(5):403.e1-5. doi: 10.1016/j.ajog.2012.08.032. Epub 2012 Aug 24. — View Citation

Osterman MJ, Martin JA. Recent declines in induction of labor by gestational age. NCHS Data Brief. 2014 Jun;(155):1-8. — View Citation

Pettker CM, Pocock SB, Smok DP, Lee SM, Devine PC. Transcervical Foley catheter with and without oxytocin for cervical ripening: a randomized controlled trial. Obstet Gynecol. 2008 Jun;111(6):1320-6. doi: 10.1097/AOG.0b013e31817615a0. — View Citation

Saccone G, Berghella V. Induction of labor at full term in uncomplicated singleton gestations: a systematic review and metaanalysis of randomized controlled trials. Am J Obstet Gynecol. 2015 Nov;213(5):629-36. doi: 10.1016/j.ajog.2015.04.004. Epub 2015 Apr 13. — View Citation

Schoen CN, Grant G, Berghella V, Hoffman MK, Sciscione A. Intracervical Foley Catheter With and Without Oxytocin for Labor Induction: A Randomized Controlled Trial. Obstet Gynecol. 2017 Jun;129(6):1046-1053. doi: 10.1097/AOG.0000000000002032. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Time to delivery The time from induction defined as the primary intervention following balloon expulsion to delivery. Up to 96 Hours
Primary Delivery within 24 hours The proportion of women that delivered within 24 hours of induction Up to 96 Hours
Secondary Cesarean delivery Cesarean delivery rates and indications Up to 96 Hours
Secondary Operative delivery Operative delivery rates and indications Up to 96 Hours
Secondary Intrapartum fever Fever >38 degrees Celsius during labor Up to 96 Hours
Secondary Postpartum fever during the postpartum hospital stay Fever >38 degrees Celsius > 24hours after delivery Up to 7 days
Secondary Post partum hemorrhage Estimation of obstetrician >500cc bleeding post partum for vaginal delivery or>1000 cc at cesarean section Up to 7 days
Secondary Neonatal outcomes- Apgar Apgar score 10 minutes
Secondary Neonatal outcomes - PH umbilical PH of vein and or artery of umbilical cord 10 minutes
Secondary Neonatal outcomes- NICU admission Admission to Neonatal Intensive Care Unit Up to 30 days
Secondary Neonatal outcomes- infection Neonatal fever/sepsis Up to 30 days
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