Key Insights

Highlights

Success Rate

100% trial completion (above average)

Clinical Risk Assessment

Based on trial outcomes

Moderate Risk

Score: 40/100

Termination Rate

0.0%

0 terminated out of 24 trials

Success Rate

100.0%

+13.5% vs benchmark

Late-Stage Pipeline

13%

3 trials in Phase 3/4

Results Transparency

0%

0 of 11 completed with results

Key Signals

100% success

Data Visualizations

Phase Distribution

21Total
Not Applicable (17)
P 2 (1)
P 4 (3)

Trial Status

Completed11
Unknown6
Recruiting4
Withdrawn1
Active Not Recruiting1
Not Yet Recruiting1

Trial Success Rate

100.0%

Benchmark: 86.5%

Based on 11 completed trials

Clinical Trials (24)

Showing 20 of 20 trials
NCT05339555Not ApplicableCompletedPrimary

IUD Self-Removal Study

NCT07295054Phase 4RecruitingPrimary

3 mL Inhaled Methoxyflurane for Intrauterine Device (IUD) Insertion

NCT07290517Not ApplicableNot Yet RecruitingPrimary

Assessing Pain and Effectiveness of Carevix Device for IUD Insertions

NCT06496854Phase 2Withdrawn

Prescribing Lorazepam for IUD Insertion: Pilot Feasibility Study

NCT06891794Not ApplicableRecruitingPrimary

Use of Cervical Cap and Menstrual Disc for Application of Topical Anesthetic Prior to IUD Insertion

NCT06240260Not ApplicableRecruitingPrimary

TENS Unit for Analgesia During IUD Insertion

NCT06864078Not ApplicableCompletedPrimary

IUCD Insertion in Patients Delivered by Cesarean Section

NCT04927741Not ApplicableCompleted

Essential Oils Following IUD Insertion

NCT02076217Active Not RecruitingPrimary

Quick Start of Highly Effective Contraception

NCT05700812Not ApplicableCompletedPrimary

IUD Placement Without Sounding

NCT05875571Phase 4RecruitingPrimary

Intravenous Ketorolac Administration to Attenuate Post-procedural Pain Associated With Intrauterine Device Placement

NCT06042556Not ApplicableCompletedPrimary

IUD Self-Removal: Evaluating an Online Guide for Self-removal in Clinical and Non-clinical Settings

NCT06023849Not ApplicableUnknownPrimary

Trans Caesarean Intra Uterine Contraceptive Device Insertion Versus Conventional Postpartum 6 Weeks Insertion

NCT04932382Not ApplicableCompletedPrimary

Misoprostol Prior to Intrauterine Device Insertion

NCT05471362UnknownPrimary

Barriers of Immediate Postpartum Intrauterine Device Uptake

NCT05383924Not ApplicableCompleted

Intrauterine Contraceptive Device Insertion During Cesarean Section (CS) Versus Delayed Insertion

NCT04539899Not ApplicableCompletedPrimary

Evaluation of the Influence of the Virtual Reality Helmet on Pain During IUD Insertion

NCT05283798Not ApplicableUnknownPrimary

Insertion of Copper T380 Versus Multiload IUD Post Partum

NCT05252117Phase 4Unknown

Uterovaginal Plexus Block With Articaine for Intrauterine Device Placement Patients Who Are Indicated for the Use of Copper IUD as a Contraceptive Method Will be Invited to Participate in This Research.

NCT05187078Not ApplicableCompletedPrimary

Allis Clamp Versus Single-tooth Tenaculum

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