Trials / Unknown
UnknownNCT04311658
Safety and Efficacy of the Effect of Isosorbide Mononitrate in Reducing Pain During Levonorgestrel-releasing Intrauterine Device Insertion
Safety and Efficacy of the Effect of Isosorbide Mononitrate in Reducing Pain During Levonorgestrel-releasing Intrauterine Device Insertion in Adolescents and Young Women
- Status
- Unknown
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 88 (estimated)
- Sponsor
- Cairo University · Academic / Other
- Sex
- Female
- Age
- 14 Years – 25 Years
- Healthy volunteers
- Not accepted
Summary
the aim of the study is to evaluate the safety and efficacy of isosorbide mononitrate vaginal administration in reducing pain during LNG-IUD insertion in adolescents and young women
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Isosorbide Mononitrate 40 MG | one tablet of Isosorbide Mononitrate (40 mg) vaginally 3 hours prior to LNG- IUD insertion |
| DRUG | Placebo | one tablet of placebo vaginally 3 hours prior to LNG-IUD insertion |
Timeline
- Start date
- 2020-03-30
- Primary completion
- 2020-06-25
- Completion
- 2020-07-05
- First posted
- 2020-03-17
- Last updated
- 2020-03-17
Source: ClinicalTrials.gov record NCT04311658. Inclusion in this directory is not an endorsement.