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NCT04041687

Outpatient Cervical Ripening

Completed Last updated 30 October 2024
What this trial tests

trial in Pregnancy in 35 participants. Completed in 1 March 2020.

Timeline
1 June 2019
Primary endpoint
1 March 2020
1 March 2020

Quick facts

Lead sponsorPrisma Health-Upstate
StatusCompleted
Study typeOBSERVATIONAL
Enrollment35
Start date1 June 2019
Primary completion1 March 2020
Estimated completion1 March 2020
Sites1 location across United States

Conditions studied

Sponsor

Prisma Health-Upstate — full company profile →

Who can join

Eligibility, female only, with Pregnancy. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The process of labor induction can mean several hours or even days spent as an inpatient prior to delivery. These prolonged hospital admissions contribute to increased financial burden on both patients and hospital systems, dissatisfaction with induction length, and staffing concerns. Several obstetric practices in the U.S. have already incorporated outpatient cervical ripening (the beginning of the induction process) into their regular practices. The investigators aim to determine if outpatient cervical ripening is a safe, non-inferior, and preferred option to the traditional inpatient induction process.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other recruiting trials for Pregnancy

Currently open trials in the same condition.

Other Prisma Health-Upstate trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04041687.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing