Success Metrics

Clinical Success Rate
88.0%

Based on 22 completed trials

Completion Rate
88%(22/25)
Active Trials
0(0%)
Results Posted
9%(2 trials)
Terminated
3(9%)

Phase Distribution

Ph phase_3
7
21%
Ph not_applicable
13
38%
Ph phase_1
1
3%
Ph phase_2
3
9%
Ph phase_4
9
26%

Phase Distribution

1

Early Stage

3

Mid Stage

16

Late Stage

Phase Distribution33 total trials
Phase 1Safety & dosage
1(3.0%)
Phase 2Efficacy & side effects
3(9.1%)
Phase 3Large-scale testing
7(21.2%)
Phase 4Post-market surveillance
9(27.3%)
N/ANon-phased studies
13(39.4%)

Highest Phase Reached

Phase 4

Trial Status & Enrollment

Completion Rate

88.0%

22 of 25 finished

Non-Completion Rate

12.0%

3 ended early

Currently Active

0

trials recruiting

Total Trials

34

all time

Status Distribution
Completed(22)
Terminated(3)
Other(9)

Detailed Status

Completed22
unknown9
Terminated3

Development Timeline

Analytics

Development Status

Total Trials
34
Active
0
Success Rate
88.0%
Most Advanced
Phase 4

Trials by Phase

Phase 11 (3.0%)
Phase 23 (9.1%)
Phase 37 (21.2%)
Phase 49 (27.3%)
N/A13 (39.4%)

Trials by Status

unknown926%
completed2265%
terminated39%

Recent Activity

Clinical Trials (34)

Showing 20 of 34 trialsScroll for more
NCT02888041Phase 3

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

Terminated
NCT02649920Not Applicable

Comparing the Efficiency of Cervical Ripening BALLoon (Cook) to the DINOprostone (Propess) for the Cervical Maturation in Case of Unfavorable Cervix (Bishop <6) in the Population of Obese Pregnant Women (BMI >= 30 kg/m²)

Terminated
NCT05761418Phase 3

Preoperative Vaginal Dinoprostone Versus Misoprostone in Abdominal Myomectomy

Completed
NCT02825641Not Applicable

Premature Rupture of Membranes With a Bishop Score<6: Comparison of Medical Induction/Expectant Management

Completed
NCT05430711Phase 4

Dinoprostone Induction vs. Expectant Management After PROM at Term

Unknown
NCT04597333Not Applicable

Labor Induction After Failed Induction With Dinoprostone.

Completed
NCT04500496Not Applicable

Vaginal Dinoprostone Versus Isonicotinic Acid Hydrazide Prior to Diagnostic Office Hysteroscopy

Unknown
NCT03001661Phase 3

An RCT of a Synthetic Osmotic Cervical Dilator for Induction of Labour in Comparison to Dinoprostone Vaginal insErt

Completed
NCT03067597Phase 3

An Open-label Trial Investigating the Efficacy and Safety of a Vaginal Insert in Pregnant Women at Term

Completed
NCT03067727Phase 3

A Randomised Trial Investigating the Efficacy and Safety of a Vaginal Insert in Pregnant Women at Term

Completed
NCT03033264Not Applicable

Labor Induction With Dinoprostone in Oppose to Cervical Ripening Balloon as a Factor of BMI.

Completed
NCT04044079Phase 4

Vaginal Dinoprostone Versus Vaginal Misoprostol Prior to Diagnostic Office Hysteroscopy in Postmenopausal Patients

Completed
NCT04079140Phase 4

Vaginal Dinoprostone Administration Prior to Intrauterine Device Insertion

Completed
NCT04080336Phase 4

Comparison of Vaginal Misoprostol and Dinoprostone Prior to Copper Intrauterine Device Insertion in Nulliparous Women

Completed
NCT04046302Phase 4

Vaginal Dinoprostone Administration Prior to an Intrauterine Device Insertion in Multiparous Women.

Completed
NCT02618096Not Applicable

Concurrent Oxytocin With Membrane Sweeping Versus Dinoprostone Pessary in Labor Induction of Multiparous Women at Term

Completed
NCT02416583Not Applicable

Concurrent Oxytocin With Membrane Sweeping Versus Dinoprostone Pessary in Labor Induction of Nulliparas at Term

Completed
NCT04045548Phase 4

Vaginal Dinoprostone Administration Prior to Insertion Levonorgestrel-releasing Intrauterine System in Women With no Previous Vaginal Delivery

Completed
NCT03675802Not Applicable

Cervical Preparation in Hysteroscopy

Unknown
NCT01720394Phase 4

Efficacy of Induction of Labor on Term Using a Double Balloon Catheter Compared to Dinoprostone Vaginal-insert

Unknown

Drug Details

Intervention Type
DRUG
Total Trials
34