Trials / Withdrawn
WithdrawnNCT02036203
A Study on the Safety and Efficacy of the SCu300A IUB Compared to the TCu380 Copper IUD
A Prospective, Randomized, Single Blind, Two Arms Controlled Study of the Safety and Efficacy of the SCu300A IUB™ Spherical Copper Intrauterine Ball in Comparison to TCu 380 IUD Intra-uterine Contraceptive Device
- Status
- Withdrawn
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 0 (actual)
- Sponsor
- Ocon Medical Ltd. · Industry
- Sex
- Female
- Age
- 25 Years – 42 Years
- Healthy volunteers
- Accepted
Summary
This study aims to evaluate the safety and efficacy of the IUB SCu300A spherical copper IUD compared to the standard T shaped copper IUD, the TCu380. Participants will be followed for one year and quality of life measurements will be measured during this period as well.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | SCu300A IUB | Spherical copper contraceptive |
| DEVICE | TCu380A IUD | T-shaped copper IUD |
Timeline
- Start date
- 2014-01-14
- Primary completion
- 2014-01-14
- Completion
- 2014-01-14
- First posted
- 2014-01-14
- Last updated
- 2018-07-06
Locations
1 site across 1 country: Israel
Source: ClinicalTrials.gov record NCT02036203. Inclusion in this directory is not an endorsement.