Trials / Completed
CompletedNCT04312048
the Effect of Isosorbide Mononitrate in Reducing Pain During Cooper Intrauterine Device Insertion
the Effect of Vaginal Isosorbide Mononitrate Administration in Reducing Pain During Cooper Intrauterine Device Insertion in Nulliparous Women : a Randomized Controlled Trial
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 110 (actual)
- Sponsor
- Cairo University · Academic / Other
- Sex
- Female
- Age
- —
- Healthy volunteers
- Not accepted
Summary
The aim of the study is to evaluate the efficacy of isosorbide mononitrate vaginal administration in reducing pain during copper IUD insertion in nulliparous women
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Isosorbide mononitrate | one tablet of Isosorbide Mononitrate (40 mg) vaginally 3 hours prior to copper IUD insertion |
| DRUG | placebo | one tablet of placebo vaginally 3 hours prior to copper IUD insertion |
Timeline
- Start date
- 2020-04-15
- Primary completion
- 2020-10-25
- Completion
- 2020-11-30
- First posted
- 2020-03-18
- Last updated
- 2021-01-20
Locations
1 site across 1 country: Egypt
Source: ClinicalTrials.gov record NCT04312048. Inclusion in this directory is not an endorsement.