Status:
UNKNOWN
Safety and Efficacy of the Effect of Isosorbide Mononitrate in Reducing Pain During Levonorgestrel-releasing Intrauterine Device Insertion
Lead Sponsor:
Cairo University
Conditions:
Contraception
Eligibility:
FEMALE
14-25 years
Phase:
PHASE3
Brief 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
Eligibility Criteria
Inclusion
- adolescents and young women requesting LNG-IUD insertion
Exclusion
- heavy vaginal bleeding,pregnancy, contraindications to IUD insertion, allergy or contraindication to isosorbide mononitrate, uterine anomaly
Key Trial Info
Start Date :
March 30 2020
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
July 5 2020
Estimated Enrollment :
88 Patients enrolled
Trial Details
Trial ID
NCT04311658
Start Date
March 30 2020
End Date
July 5 2020
Last Update
March 17 2020
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