Key Insights

Highlights

Success Rate

100% trial completion (above average)

Clinical Risk Assessment

Based on trial outcomes

Moderate Risk

Score: 50/100

Termination Rate

0.0%

0 terminated out of 17 trials

Success Rate

100.0%

+13.5% vs benchmark

Late-Stage Pipeline

6%

1 trials in Phase 3/4

Results Transparency

7%

1 of 15 completed with results

Key Signals

1 with results100% success

Data Visualizations

Phase Distribution

17Total
Not Applicable (13)
Early P 1 (1)
P 1 (2)
P 4 (1)

Trial Status

Completed15
Not Yet Recruiting1
Unknown1

Trial Success Rate

100.0%

Benchmark: 86.5%

Based on 15 completed trials

Clinical Trials (17)

Showing 17 of 17 trials
NCT07094555Not ApplicableNot Yet RecruitingPrimary

The Effect of Two Different Interventions Applied During the Transfer of Children to the Operating Room for Circumcision on Fear, Anxiety, Comfort and Pain Levels

NCT04263064Early Phase 1CompletedPrimary

High Volume Caudal Study

NCT03914365Not ApplicableUnknownPrimary

Pudendal Nerve Block vs Penile Nerve Block for Analgesia During Pediatric Circumcision

NCT03223532Not ApplicableCompletedPrimary

Randomized Trial Comparing PrePex Day 7 Foreskin Removal Procedure (FRP) to a Day 0 PrePex FRP .

NCT02091726Not ApplicableCompletedPrimary

Phase 4 Field Trial of the Unicirc Instrument With Tissue Adhesive

NCT03634358Not ApplicableCompletedPrimary

Bipolar Scissors for Circumcision

NCT02277795Not ApplicableCompletedPrimary

Evaluation of the AccuCirc for Early Infant Male Circumcision in Nyanza, Kenya

NCT02242565Not ApplicableCompletedPrimary

Safety and Effectiveness of Different ShangRing Device Sizes for Adult Male Circumcision in Lusaka, Zambia

NCT02167776Not ApplicableCompletedPrimary

From Obstacles to Opportunities for Male Circumcision in Tanzania

NCT02309710Phase 1CompletedPrimary

Male Circumcision (MC) Using the ShangRing™ Device in Malawi

NCT01247844Not ApplicableCompletedPrimary

Evaluation of Healing at Three Time Intervals and Potential for Spontaneous Detachment

NCT02281435Not ApplicableCompletedPrimary

Follow Up Study to Evaluate a Non-Surgical Device for Adult Male Circumcision for Screen Failure Subjects

NCT01434628Not ApplicableCompletedPrimary

Cohort Field Study to Assess the Safety and Efficacy of the PrePex Device for Non-Surgical Circumcision When Performed by Nurses

NCT01921608Not ApplicableCompletedPrimary

Safety Study of the PrePex Device for Non-Surgical Adult Male Circumcision During Phased in National Implementation in an Effort to Prevent the Spread of HIV

NCT01567436Phase 4CompletedPrimary

A Prospective Field Study: Introducing the Shang Ring in Routine Clinical Settings

NCT01150370Not ApplicableCompletedPrimary

A Pivotal Study to Assess the Safety and Efficacy of The PrePex System, a Male Circumcision Device and Methodology for Rapid Scale up of Painless and Bloodless National Circumcision Programs, in Urban and Remote Rural Settings

NCT00993811Phase 1CompletedPrimary

The Shang Ring: A Novel Male Circumcision Device for HIV Prevention

Showing all 17 trials

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