Clinical Trials Logo
  1. Home
  2. Labor, Obstetric
  3. NCT05109247

Prediction of Spontaneous Onset of Labor at Term — PREDICT  

Labor, Induced Clinical Trial

Official title:
Prediction of Spontaneous Onset of Labor at Term

Clinical Trial Summary

The study intends to develop a predictive model of spontaneous onset of labor between 39 and 41 weeks of pregnancy in women carrying singletons and without indication of delivery before this date. The main hypothesis is that a combination of clinical, ultrasonographic, biochemical and/or biophysical variables will allow to differentiate women who will spontaneously trigger their labors from those who will require an induction by the term of their pregnancies. A tool of this kind should aid in the individualization of the management of the final weeks of pregnancy and, at the light of recent evidence, provide support to the decision-making processes.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05109247
Study type Observational [Patient Registry]
Source University Hospital, Geneva
Contact
Status Completed
Phase
Start date August 22, 2019
Completion date December 31, 2022
View Details
See also
  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
Terminated NCT02373800 - Elastography for Evaluating Cervical Maturity in Preparation for Labor Induction at 37 to 42 Weeks of Gestation