Prehospital Cervical Ripening Before Induction and the Maternal Experience (PRIME)
Randomized Controlled Trial of Prehospital Cervical Ripening With an Outpatient Transcervical Foley Balloon and the Duration of Induction and Maternal Satisfaction
Sponsor: University of California, San Francisco
Terminated
Inadequate enrollment. Key study personnel transitioned to a different role.
Other terminated trials from University of California, San Francisco
- Hypertension · Phase PHASE2 · Jan 2026
- Menstrual Irregularity · Phase PHASE4 · Sep 2025
- Diabetes Mellitus, Type 2 · Phase NA · Feb 2025
- Asthma · Phase PHASE4 · Feb 2025
- Stone, Kidney · Phase NA · Dec 2024
See all terminations from University of California, San Francisco
Other Cervical Ripening trials with similar outcome
A NA clinical study on Cervical Ripening and Labor, Induced, this trial is terminated or withdrawn. The trial is conducted by University of California, San Francisco and has accumulated 7 data snapshots since 2012. Longitudinal tracking of this trial contributes to a broader understanding of treatment development timelines.
Status Flow
Change History
7 versions recorded-
Sep 2024 — Present [monthly]
Terminated NA
-
Jul 2024 — Sep 2024 [monthly]
Terminated NA
-
Jan 2021 — Jul 2024 [monthly]
Terminated NA
-
Sep 2020 — Jan 2021 [monthly]
Terminated NA
-
Jan 2020 — Sep 2020 [monthly]
Terminated NA
Status: Unknown Status → Terminated · Phase: PHASE1_PHASE2 → NA
▶ Show 2 earlier versions
-
Jun 2018 — Jan 2020 [monthly]
Unknown Status PHASE1_PHASE2
-
Jan 2017 — Jun 2018 [monthly]
Unknown Status PHASE1_PHASE2
First recorded
Jul 2012
Trial started
Per CT.gov start date — pre-dates our first snapshot
Eligibility Summary
No eligibility information available.
Contact Information
- University of California, San Francisco
For direct contact, visit the study record on ClinicalTrials.gov .