Key Insights

Highlights

Success Rate

92% trial completion (above average)

Clinical Risk Assessment

Based on trial outcomes

Moderate Risk

Score: 30/100

Termination Rate

4.9%

3 terminated out of 61 trials

Success Rate

92.1%

+5.6% vs benchmark

Late-Stage Pipeline

38%

23 trials in Phase 3/4

Results Transparency

29%

10 of 35 completed with results

Key Signals

10 with results92% success

Data Visualizations

Phase Distribution

58Total
Not Applicable (29)
P 2 (6)
P 3 (14)
P 4 (9)

Trial Status

Completed35
Unknown8
Recruiting5
Not Yet Recruiting4
Withdrawn4
Terminated3

Trial Success Rate

92.1%

Benchmark: 86.5%

Based on 35 completed trials

Clinical Trials (61)

Showing 20 of 20 trials
NCT07214948Not ApplicableNot Yet Recruiting

Open, Randomized Feasibility Trial on the Safety and Performance of the INGA Catheter for Labor Induction

NCT07414771Not ApplicableNot Yet Recruiting

Safety and Usability of the Inga Catheter for Labor Induction (INGA-MDP)

NCT07559812Not ApplicableActive Not Recruiting

Comparison of Vaginal PGE2 (Dinoprostone) and Vaginal Misoprostol for Induction of Labour in Primigravid Term Pregnancy

NCT06591247Not ApplicableRecruiting

Membrane Stripping for Cervical Ripening

NCT07432282Not ApplicableNot Yet Recruiting

Evaluation of the INGA Sensor System for Fetal and Uterine Monitoring During Cervical Ripening

NCT07366359Not ApplicableRecruiting

PGE2 Followed by Oxytocin vs Oxytocin in Term PROM (POXY-PROM)

NCT07317674Not ApplicableNot Yet Recruiting

Combined Nipple Stimulation and Foley Balloon for Cervical Ripening

NCT06809985Not ApplicableCompleted

Latent Phase Membrane Stripping for Caesarean Section Reduction

NCT04949633Phase 3RecruitingPrimary

Oxytocin vs Prostaglandins for Labor Induction of Women With an Unfavorable Cervix After 24h of Cervical Ripening

NCT00545194Phase 3WithdrawnPrimary

Cervical Ripening Before Induction of Labour at Term: a Randomised Comparison of Prostin vs Propess

NCT07043088Not ApplicableRecruiting

The SWEEP Trial: a Randomized Controlled Trial

NCT07121634Not ApplicableActive Not RecruitingPrimary

Cervical Ripening With Misoprostol vs Isosorbide Mononitrate ; A Parallel -Arm Randomized Controlled Trial

NCT02975167Not ApplicableCompleted

Patient Satisfaction During Outpatient Versus Inpatient Foley Catheter Induction of Labor

NCT05864326Not ApplicableCompletedPrimary

Heated Saline in Cervical Balloon for Labor Induction, a RCT

NCT06726278Not ApplicableCompleted

Significance of Misoprostol-induced Cervical Ripening Prior to Hysteroscopy

NCT06623175Not ApplicableCompleted

Effects of Acupuncture in Spontaneous Rapture of Membranes: Applicability and Effectiveness

NCT02888041Phase 3TerminatedPrimary

Is There an Interest in Repeating the Vaginal Administration of Dinoprostone (Propess®), to Promote Induction of Labor of Pregnant Women at Term?

NCT05096104CompletedPrimary

Patient Satisfaction During Artificial Induction of Labor by Cervical Ripening

NCT02465164Not ApplicableCompletedPrimary

Cervical Ripening With Cook Catheter Plus Low Dose Oxytocin

NCT04773314CompletedPrimary

General Drug Use-results Survey on PROPESS Vaginal Inserts in Treatment for Initiation of Cervical Ripening in Patients at Term (From 37 Completed Weeks of Gestation)

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