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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

TypeNameDescription
DRUGIsosorbide Mononitrate 40 MGone tablet of Isosorbide Mononitrate (40 mg) vaginally 3 hours prior to LNG- IUD insertion
DRUGPlaceboone 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.

Safety and Efficacy of the Effect of Isosorbide Mononitrate in Reducing Pain During Levonorgestrel-releasing Intrauterin (NCT04311658) · Clinical Trials Directory