CompletedPhase 3

the Effect of Isosorbide Mononitrate in Reducing Pain During Cooper Intrauterine Device Insertion

Egypt110 participantsStarted 2020-04-15

Plain-language 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

Who can participate

SexFEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * nulliparous women requesting copper IUD device insertion Exclusion Criteria: * parous women, contraindications to IUD insertion, allergy or contraindication to isosorbide mononitrate, uterine anomaly

What they're measuring

pain during IUD insertion

Timeframe: 5 minutes

Trial details

NCT IDNCT04312048

SponsorCairo University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2020-10-25

View on ClinicalTrials.gov More IUD Insertion Pain trials