Labor, Induced Clinical Trial
Official title:
Elastography for Evaluating Cervical Maturity in Preparation for Labor Induction at 37 to 42 Weeks of Gestation
The primary objective of this study is to determine if a cervical hardness score (determined by cervical ultrasound with elastography) can predict delivery mode (vaginal versus cesarian for slow dilatation (more than 2-3h without fetal suffering) regardless of the induction mode (ocytocin alone or with an intravaginal device releasing PGE2).
The secondary objectives of this study are:
A. To determine composite criteria (combining elastographic, parity and Bishop score
information) that predict delivery mode.
B. To determine the prognostic value of elastography as concerns delivery within 24 hours
among patients induced via oxytocin with an intravaginal device releasing PGE2 (Bishop score
< 6).
C. To determine the prognostic value of elastography as concerns delivery mode (vaginal
versus cesarian for slow dilatation (more than 2-3h without fetal suffering))among patients
induced via oxytocin alone.
D. To evaluate the intra- and inter-operator reproducibility of the cervical hardness score
determined via elastography.
E. To evaluate the economic impact of using the cervical hardness score from the point of
view of the French social system (French health insurance) and the hospital.
;
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT02902653 -
Efficacy and Safety of Hourly Titrated Misoprostol Versus Vaginal Dinoprostone and Misoprostol for Cervical Ripening and Labor Induction
|
Phase 4 | |
Completed |
NCT05100264 -
Effect of Acidic Vaginal pH on the Efficacy of Dinoprostone for Labor Induction
|
N/A | |
Completed |
NCT01962831 -
Randomized Controlled Trial: Induction of Labour of Obese Women With Dinoprostone or Single Balloon Catheter
|
N/A | |
Recruiting |
NCT05857059 -
Misoprostol for Induction of Labor in Obese Women: Comparison Between 25 and 50 mcg Oral Administration
|
N/A | |
Completed |
NCT03665688 -
Comparing Outpatient to Inpatient Cervical Ripening Using Dilapan-S®
|
N/A | |
Completed |
NCT00992524 -
Oral Titrated Misoprostol for Induction of Labour
|
N/A | |
Completed |
NCT00259103 -
Recombinant Human Relaxin (rhRlx) in Pregnant Women Scheduled for Induction of Labor
|
Phase 2 | |
Completed |
NCT04755218 -
Labor Induction With Oral Versus Vaginal Misoprostol
|
||
Completed |
NCT04746248 -
Outpatient Labor Induction Using Oral Misoprostol in Norway
|
N/A | |
Completed |
NCT05838313 -
Should I Have an Elective Induction?
|
N/A | |
Completed |
NCT03140488 -
Oxytocin Dosage to Decrease Induction Duration
|
Phase 4 | |
Recruiting |
NCT02486679 -
A Trial of Prostaglandin E2 Tablets Versus Foley Catheter for Labor Induction
|
Phase 4 | |
Terminated |
NCT01641601 -
Prehospital Cervical Ripening Before Induction and the Maternal Experience
|
N/A | |
Completed |
NCT00465998 -
Study of Ultrasound Imaging to Predict Time and Outcome in Pregnancies With Induced Labor
|
N/A | |
Completed |
NCT00393731 -
A Randomized, Control Trial for Preinduction Cervical Ripening
|
Phase 2 | |
Completed |
NCT00545194 -
Cervical Ripening Before Induction of Labour at Term: a Randomised Comparison of Prostin vs Propess
|
Phase 3 | |
Completed |
NCT05874024 -
Induction of Labour With a Double Balloon Catheter
|
||
Completed |
NCT03407625 -
Foley Bulb With Oral Misoprostol for Induction of Labor
|
N/A | |
Completed |
NCT04731896 -
Early Versus Late Amniotomy During Labor Induction in Women With Bishop's Score of ≥ 6
|
N/A | |
Completed |
NCT05885087 -
'Extended Balloon Catheter' Labour Induction; a Single Arm Pilot Trial'
|
N/A |