Simplified IUD Insertion Technique
NCT02733081 · Status: WITHDRAWN · Phase: NA · Type: INTERVENTIONAL
Last updated 2022-12-05
Summary
This is a randomized controlled trial that compares traditional IUD insertion with that of a no uterine sound, no bimanual pelvic exam approach. The investigators hypothesis is that IUD placement is safe and effective without pre-procedural assessment of uterine size, direction, or depth.
Conditions
- Contraception
Interventions
- PROCEDURE
-
Simplified IUD Insertion
IUD Insertion with no bimanual pelvic exam or uterine sounding.
Sponsors & Collaborators
- lead OTHER
Principal Investigators
-
Paul D Blumenthal, MD, MPH · Stanford University
Study Design
- Allocation
- RANDOMIZED
- Purpose
- PREVENTION
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- FEMALE
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2018-01-01
- Primary Completion
- 2020-10-31
- Completion
- 2020-10-31
More Related Trials
-
Pilot Study of Suction as a Mechanism of IUD Expulsion With Concomitant Menstrual Cup Use
NCT05254041 ·Status: RECRUITING ·Phase: NA
-
Novel Cervical Retraction Device
NCT02283463 ·Status: UNKNOWN ·Phase: NA
-
A Randomized Controlled Trial of No Strings Intrauterine Device (IUD) Removal Techniques
NCT05702242 ·Status: ACTIVE_NOT_RECRUITING ·Phase: NA
-
Establishing Immunogenicity and Safety of Needle-free Intradermal Delivery of mRNA COVID-19 Vaccine
NCT05315362 ·Status: UNKNOWN ·Phase: PHASE2
-
Intrauterine Device (IUD) Self Removal
NCT05191238 ·Status: TERMINATED ·Phase: NA
-
Allis Clamp Versus Single-tooth Tenaculum
NCT05187078 ·Status: COMPLETED ·Phase: NA
-
FemBloc® Permanent Contraception - Confirmation Feasibility Trial
NCT04273594 ·Status: ACTIVE_NOT_RECRUITING ·Phase: NA
-
Removal of Palpable Subdermal Contraceptive Rod Implants.
NCT02986971 ·Status: TERMINATED ·Phase: NA
-
Comparative Study of the VeraCept Low-Dose Intrauterine Copper Contraceptive vs. the TCu380 Copper IUD
NCT02167763 ·Status: COMPLETED ·Phase: PHASE1
-
Pain Perception With Tenaculum Placement
NCT02969421 ·Status: COMPLETED ·Phase: NA
-
Usability, Safety and Efficacy of AspivixTM (Comparative Study)
NCT04441281 ·Status: COMPLETED ·Phase: NA
-
Usability, Safety and Efficacy of AspivixTM
NCT04441333 ·Status: COMPLETED ·Phase: NA
-
Pilot Removal of Palpable Subdermal Contraceptive Rod Implants
NCT03356119 ·Status: TERMINATED ·Phase: NA
-
Assessment of the INVOcell Culture Device When Used for up to Five-Day Incubation
NCT04644380 ·Status: COMPLETED ·Phase: NA
-
Preliminary Evaluation of a "Clip" Device for Contraceptive Implant Removal
NCT04919395 ·Status: TERMINATED ·Phase: NA
-
Clinical Precision and In-use Analyte Stability Study for 19 Parameters in Adult Arterial Whole Blood for PICO70 and SafePICO
NCT06823648 ·Status: COMPLETED
-
A Trial for the Safety and Effectiveness of a Novel Antimicrobial-Coated Foley Catheter for Reduction of CAUTI.
NCT01681511 ·Status: TERMINATED ·Phase: NA
-
Comparison of an Antibiotic Impregnated PICC Catheter Versus a Regular PICC Catheter in a Tertiary Care Setting
NCT01765738 ·Status: WITHDRAWN ·Phase: PHASE2
-
Evaluation of the Safety and Efficacy of Single-use Precision Filtered Infusion Sets for Intravenous Infusion
NCT04962516 ·Status: COMPLETED
-
Essure (Model ESS310) Placement Rate Study
NCT02064413 ·Status: COMPLETED ·Phase: PHASE3
-
Long-Term Assessment of the Safety and Performance of the NuVasive Simplify Disc at Two Levels
NCT05691231 ·Status: ENROLLING_BY_INVITATION
-
Safety and Performance of a New Coating for Urinary Intermittent Catheters
NCT01800903 ·Status: COMPLETED ·Phase: NA
-
Investigation to Evaluate Performance and Safety of RemovAid ™ in Removal of Contraceptive Implants
NCT03912649 ·Status: TERMINATED ·Phase: NA
-
Post Marketing Surveillance of the CentrosFLO™ Tunneled IJ Catheter
NCT02349308 ·Status: COMPLETED
-
Clinical Trial of New Single-use Compact Intermittent Catheter
NCT05841004 ·Status: COMPLETED ·Phase: NA