Key Insights

Highlights

Success Rate

86% trial completion

Clinical Risk Assessment

Based on trial outcomes

Moderate Risk

Score: 42/100

Termination Rate

8.5%

4 terminated out of 47 trials

Success Rate

86.2%

-0.3% vs benchmark

Late-Stage Pipeline

40%

19 trials in Phase 3/4

Results Transparency

12%

3 of 25 completed with results

Key Signals

3 with results86% success

Data Visualizations

Phase Distribution

38Total
Not Applicable (12)
P 1 (2)
P 2 (5)
P 3 (7)
P 4 (12)

Trial Status

Completed25
Unknown14
Terminated4
Withdrawn3
Suspended1

Trial Success Rate

86.2%

Benchmark: 86.5%

Based on 25 completed trials

Clinical Trials (47)

Showing 20 of 20 trials
NCT06333691Not ApplicableCompletedPrimary

Comparative Study Between Calcium Gluconate With Diosmin, Cabergoline and Cabergoline With Diosmin

NCT02686151Phase 3UnknownPrimary

The Letrozole Administration During Luteal Phase

NCT05362734CompletedPrimary

Freeze All Strategy Versus Fresh Embryo Transfer After GnRH Analogue Trigger

NCT05638529Phase 4UnknownPrimary

Dual Trigger" in IVF Patients at High Risk of Ovarian Hyper Stimulation Syndrome

NCT05588635CompletedPrimary

Association Between Live Birth Rate and Serum Progesterone During Hormonal Replacement Therapy

NCT03794037Phase 2SuspendedPrimary

Montelukast for Prevention & Treatment of OHSS

NCT05198128Not ApplicableUnknownPrimary

Ovarian Hyperstimulation Syndrome Using Calcium Infusion

NCT03876145Not ApplicableCompleted

The Four Methods of Ovarian Stimulation in Patients With Polycystic Ovarian Syndrome

NCT04797338Phase 4Unknown

Gonadotropin Releasing Hormone Agonist (GnRHa) Versus Estrogen and Progesterone for Luteal Support in High Responders

NCT02200952CompletedPrimary

Luteal Phase Supplementation With Recombinant LH After GnRh Agonist Oocytes Triggering in Women at Risk of OHSS

NCT02610608TerminatedPrimary

Medical Assistance for the Procreation and Risk of Thrombosis.

NCT04351126Phase 2CompletedPrimary

Management of Ovarian Hyperstimulation Syndrome as a State of Defective Mineralocorticoid Response

NCT03996434Phase 4CompletedPrimary

Coasting Versus Antagonist Protocol in Patients at High Risk of OHSS

NCT02701452Not ApplicableTerminatedPrimary

Ovarian Hyperstimulation Syndrome in Patients Triggered by GnRH Agonist for Excessive Follicular Response

NCT01606709Phase 4Terminated

Gene Expression Profile After Gonadotropin Releasing Hormone (GnRH) Agonist Trigger of Oocyte Maturation

NCT01815138Phase 4CompletedPrimary

Co-administration of Low Dose hCG at the Time of GnRH Agonist Trigger or 35 Hours Later for the Prevention of OHSS

NCT01535859Phase 3CompletedPrimary

Study of Cabergoline for Prevention of Ovarian Hyperstimulation Syndrome (OHSS) in In Vito Fertilization Cycles and Derivation of OHSS Biomarkers

NCT02620605Phase 3UnknownPrimary

The Influence of Timing of Cabergoline Initiation on Prevention of OHSS

NCT03188471Phase 4UnknownPrimary

Preventive Application of GnRH Antagonist on Early OHSS

NCT03071172Phase 3UnknownPrimary

Clinical Study of Recombinant Human Follitropin for Injection Assisted in COH Assisted IVF-ET

Scroll to load more

Research Network

Activity Timeline