Clinical trial
A Post Market Surveillance Study of the Performance and Safety of UT 380® Contraceptive Intra Uterine Device in Nulliparous, Uniparous and Multiparous Women
NCT03642171 is registered in ClinicalTrials.gov with Quanta Medical as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- A Post Market Surveillance Study of the Performance and Safety of UT 380® Contraceptive Intra Uterine Device in Nulliparous, Uniparous and Multiparous Women
- Lead sponsor
- Quanta Medical
- Phase
- Observational
- Overall status
- Completed
- Start date
- July 26, 2018
- Completion date
- September 23, 2024
- Enrollment
- 200 (actual)
- Sites
- 1
Conditions
As the registry lists them; a condition with its own page is linked.
contraceptive; complications, intrauterine