WHO ICTRP trial
Comparative study on the safety and acceptability of post-delivery intrauterine…
CTRI/2016/03/006771 · Clinical Trials Registry India (CTRI) · Not Recruiting
Key facts
| Trial ID | CTRI/2016/03/006771 |
|---|---|
| Public title | Comparative study on the safety and acceptability of post-delivery intrauterine contraceptive device using standard approach (Forceps) and a new device (Inserter). |
| Scientific title | Single blinded, randomized, comparative study on the safety and acceptability of PPIUCD insertion using Kellyâ??s forceps and a dedicated PPIUCD inserter |
| Primary sponsor | USAID |
| Registry | Clinical Trials Registry India (CTRI) |
| Recruitment status | Not Recruiting |
| Study type | Interventional |
| Phase | Phase 3 |
| Countries | India |
| Interventions | Intervention1: PPIUCD Inserter: New Device to be used for post partum IUCD insertion Control Intervention1: Kellys forceps: Currently providers are using forceps for PPIUD insertion |
| Registration date | Mar 30, 2016 |
| Target size | 500 |
| Secondary IDs | NIL |
| Registry page | ctri.nic.in |
At a glance
- No Results available
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About WHO ICTRP trial registrations
The WHO ICTRP combines trial registrations from primary registries worldwide into a single searchable index. Contact and ethics-committee details are not shown here.
Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date: