Trials / Completed
CompletedNCT04339348
Comparative Safety and Efficacy of Vaginal Misoprostol Versus Lidocaine-prilocaine Cream in Levonorgestrel IUD Insertion
Comparative Safety and Efficacy of Vaginal Misoprostol Versus Lidocaine-prilocaine Cream in Reducing Pain During Levonorgestrel IUD Insertion in Women Delivered Only by Cesarean Deliveries
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 210 (actual)
- Sponsor
- Cairo University · Academic / Other
- Sex
- Female
- Age
- —
- Healthy volunteers
- Accepted
Summary
the aim of the present study is to compare the safety and Efficacy of vaginal misoprostol versus Lidocaine-prilocaine cream in reducing pain during levonorgestrel IUD Insertion in women delivered only by cesarean deliveries
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | vaginal misoprostol | vaginal misoprostol 200 mcg will be given 3 hours before LNG-IUD insertion plus inert placebo cream vaginally at the time of LNG-IUD insertion |
| DRUG | Lidocaine-Prilocaine Topical cream | Lidocaine-Prilocaine cream will be applied on the cervix at the time of LNG-IUD insertion plus vaginal placebo tablet 3 hours before LNG-IUD insertion |
| DRUG | placebo | inert placebo cream will be applied on the cervix at the time of LNG-IUD insertion plus vaginal placebo tablet 3 hours before LNG-IUD insertion |
Timeline
- Start date
- 2020-04-30
- Primary completion
- 2021-02-01
- Completion
- 2021-03-01
- First posted
- 2020-04-09
- Last updated
- 2021-05-07
Locations
1 site across 1 country: Egypt
Source: ClinicalTrials.gov record NCT04339348. Inclusion in this directory is not an endorsement.