Key Insights

Highlights

Success Rate

82% trial completion

Clinical Risk Assessment

Based on trial outcomes

Moderate Risk

Score: 49/100

Termination Rate

10.5%

2 terminated out of 19 trials

Success Rate

81.8%

-4.7% vs benchmark

Late-Stage Pipeline

11%

2 trials in Phase 3/4

Results Transparency

44%

4 of 9 completed with results

Key Signals

4 with results82% success

Data Visualizations

Phase Distribution

17Total
Not Applicable (12)
P 1 (1)
P 2 (2)
P 4 (2)

Trial Status

Completed9
Unknown4
Recruiting2
Terminated2
Not Yet Recruiting1
Withdrawn1

Trial Success Rate

81.8%

Benchmark: 86.5%

Based on 9 completed trials

Clinical Trials (19)

Showing 19 of 19 trials
NCT06537089Not ApplicableCompletedPrimary

Comparative Study Between Using WHO Labour Care Guide & Modified WHO Partograph

NCT06164613Phase 2RecruitingPrimary

Use of Cinnamomum Verum for Induction of Labor. Double Blind Randomized Clinical Trial

NCT04000438Phase 2CompletedPrimary

Effect of Tafoxiparin on Cervical Ripening and Induction of Labor in Term Pregnant Women With an Unripe Cervix

NCT04933708Not ApplicableCompletedPrimary

LaPPS: Labor Podcast for Patient Satisfaction

NCT05791630Not ApplicableRecruiting

The Norwegian World Health Organisation Labour Care Guide Trial (NORWEL)

NCT06547437Not ApplicableNot Yet Recruiting

Papaverine and Oxytocin vs Oxytocin Alone in Labor Induction

NCT03670836Phase 4CompletedPrimary

Comparison of Misoprostol Ripening Efficacy With Dilapan

NCT05262738Phase 4Completed

Misoprostol Dosing in BMI Greater Than 30

NCT04271722Not ApplicableCompleted

Clinical Evaluation of Cervical Ripening in the Outpatient Setting

NCT06343480Not ApplicableCompletedPrimary

Misoprostol Versus Oxytocin for Induction of Labour in Parturients With Spontaneous Rupture of Fetal Membranes at Term

NCT06151925Not ApplicableCompletedPrimary

Laminaria Tents Versus Vaginal Prostaglandin in Cervical Ripening

NCT04564196TerminatedPrimary

Breath Metabolomics in the Laboring Parturient

NCT04504682Not ApplicableTerminated

Ambulation With Labor Epidural in Obese Women

NCT05255263Not ApplicableWithdrawnPrimary

Goal-directed Labor Epidural Analgesia Maintenance

NCT05489315Not ApplicableUnknownPrimary

Quantifying the Impact of the Peanut Ball on the Duration of the Active Stage of Labor

NCT05510310Phase 1UnknownPrimary

Breast Stimulation vs. Low Dose Oxytocin Augmentation for Labor Induction

NCT05084326CompletedPrimary

Engagement of Fetal Head as a Predictor of a Successful Vaginal Delivery in Primigravidas Presented in Early Labor.

NCT03985618Not ApplicableUnknown

The MODE Trial: Planned Caesarean Section Versus Induction of Labour for Women With Class III Obesity

NCT03784092Not ApplicableUnknownPrimary

Effect Mobility During Induction of Labor on Time to Delivery. A Randomized Controlled Trial

Showing all 19 trials

Research Network

Activity Timeline