Trial · NCT02907060

Mechanical cervicAl ripeninG for Women With PrOlongedPregnancies

NCT02907060, Phase 3, Completed, University Hospital, Tours

3 sourcestrials-2026-11-12-0.4.0

Cite this record

ConductScience Library. Mechanical cervicAl ripeninG for Women With PrOlongedPregnancies. Trials, record NCT02907060. Release trials-2026-11-12-0.4.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT02907060

On this page

Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title: Mechanical cervicAl ripeninG for Women With PrOlongedPregnancies
NCT number: NCT02907060
Status: Completed
Phases: Phase 3
Enrollment: 1,224 participants, actual
Lead sponsor: University Hospital, Tours
Conditions: Prolonged Pregnancy
Interventions: Mechanical cervical ripening, Pharmacological cervical ripening
First posted: 2016-09-20
Last updated: 2025-12-22

Source ClinicalTrials.gov

Registered outcomes22

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

List	Outcome	Time frame	Description
Primary	Caesarean section rate for non-reassuring fetal status.	Up to 2 days after cervical ripening	Indication of the caesarean section will be settled by an adjudication committee at the end of the study
Secondary	Time between cervical ripening and delivery in hours	Up to 2 days after cervical ripening	Evaluation of time between cervical ripening and delivery in hours
Secondary	Delivery rate after 12 and 24 hours of cervical ripening	up to 2 days after cervical ripening	Evaluation of delivery rate after 12 and 24 hours of cervical ripening
Secondary	Induction with oxytocin	up to 2 days after cervical ripening	yes/no
Secondary	Total dose of oxytocin required for induction of labour	up to 2 days after cervical ripening	evaluation of total dose of oxytocin required for induction of labour
Secondary	Uterine hyper stimulation defined as more than 6 contractions by 10 minutes over a 30 minutes period	up to 2 days after cervical ripening	uterine hyperstimulation
Secondary	Requirement for tocolysis during cervical ripening or during labour	up to 2 days after cervical ripening	requirement for tocolysis
Secondary	Suspicious or pathological fetal heart rate	up to 2 days after cervical ripening	FIGO classification
Secondary	Uterine rupture	up to 2 days after cervical ripening	yes/no
Secondary	Use of analgesics during labour	up to 2 days after cervical ripening	yes/no

1 to 10 of 22Source ClinicalTrials.gov

See all 22 registered outcomes

Outcomes0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

None in this release.

Results by group0

Each measurement the trial posted, group by group, in the words and numbers it posted.

None in this release.

Participant flow0

How many started, completed or left each group, period by period.

None in this release.

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals0

The totals the trial posted for each group.

None in this release.

Papers3

The papers the trial lists on ClinicalTrials.gov.

PMID	Listed as	Source
28912192	DERIVED	PubMed
33571294	RESULT	PubMed
36996264	DERIVED	PubMed

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov: 2026-11-12; ClinicalTrials.gov
Results, from AACT: 2026-03-23; AACT
NIH grant links: 2026-11-13; NIH RePORTER

Sources 3

ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
ClinicalTrials.govNo license stated
NIH RePORTER's clinical studies and project filesPublic domain

Each source's terms

ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
ClinicalTrials.govnone stated
NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT02907060

GET https://conductscience.org/api/trials/v1/NCT02907060/registered?page=2

API reference For AI assistants