Success Metrics

Clinical Success Rate
100.0%

Based on 6 completed trials

Completion Rate
100%(6/6)
Active Trials
0(0%)
Results Posted
50%(3 trials)

Phase Distribution

Ph not_applicable
7
78%
Ph phase_2
1
11%
Ph phase_4
1
11%

Phase Distribution

0

Early Stage

1

Mid Stage

1

Late Stage

Phase Distribution9 total trials
Phase 2Efficacy & side effects
1(11.1%)
Phase 4Post-market surveillance
1(11.1%)
N/ANon-phased studies
7(77.8%)

Highest Phase Reached

Phase 4

Trial Status & Enrollment

Completion Rate

100.0%

6 of 6 finished

Non-Completion Rate

0.0%

0 ended early

Currently Active

0

trials recruiting

Total Trials

9

all time

Status Distribution
Completed(6)
Other(3)

Detailed Status

Completed6
unknown3

Development Timeline

Analytics

Development Status

Total Trials
9
Active
0
Success Rate
100.0%
Most Advanced
Phase 4

Trials by Phase

Phase 21 (11.1%)
Phase 41 (11.1%)
N/A7 (77.8%)

Trials by Status

unknown333%
completed667%

Recent Activity

0 active trials
Showing 5 of 9
completednot_applicable

Misoprostol Prior to Intrauterine Device Insertion

NCT04932382
completednot_applicable

Early vs. Interval Postpartum IUD Insertion

NCT03462758
unknownnot_applicable

Insertion of Copper T380 Versus Multiload IUD Post Partum

NCT05283798
completednot_applicable

A Study to Evaluate the Safety and Initial Efficacy of a Novel Intrauterine Device

NCT01590563
unknownphase_4

Tramadol Versus Celecoxib in Reducing Pain Associated With IUD Insertion

NCT02827487
View all 9 trials

Clinical Trials (9)

Showing 9 of 9 trials
NCT04932382Not Applicable

Misoprostol Prior to Intrauterine Device Insertion

Completed
NCT03462758Not Applicable

Early vs. Interval Postpartum IUD Insertion

Completed
NCT05283798Not Applicable

Insertion of Copper T380 Versus Multiload IUD Post Partum

Unknown
NCT01590563Not Applicable

A Study to Evaluate the Safety and Initial Efficacy of a Novel Intrauterine Device

Completed
NCT02827487Phase 4

Tramadol Versus Celecoxib in Reducing Pain Associated With IUD Insertion

Unknown
NCT03724708Not Applicable

Comparing Expulsion Rates for Different Intrauterine Device Insertion Techniques

Unknown
NCT02595125Not Applicable

Study Assessing the Reduction of Pain Felt During Installation Intra- Uterine Device by Direct Technique

Completed
NCT02841826Phase 2

Evaluation of a Novel and Simplified Technique for Intrauterine Contraceptive Devices Insertion: a Prospective Cohort Study

Completed
NCT01309919Not Applicable

Bleeding Patterns and Complications After Postpartum IUD Placement: a Pilot Study

Completed

All 9 trials loaded

Drug Details

Intervention Type
DEVICE
Total Trials
9