CompletedNot Applicable

The Role of Lidocaine Spray in Reducing Pain During Intrauterine Device Application

Turkey (Türkiye)90 participantsStarted 2022-07-01

Plain-language summary

Investigators aimed to investigate the effectiveness of the use of local lidocaine spray application to make routine intrauterine intrauterine device application more painless.

Who can participate

Age range18 Years – 45 Years

SexFEMALE

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

Inclusion Criteria: * 18-45 years old patient who comes to have an intrauterine device inserted voluntarily * The patient who gave consent to participate in the study Exclusion Criteria: * Patients who cannot have an intrauterine device because of fibroids or cervical stenosis * Patient who did not want to participate in the study

What they're measuring

Pain component

Timeframe: 1 hour

Trial details

NCT IDNCT07155785

SponsorKanuni Sultan Suleyman Training and Research Hospital

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2023-02-20

View on ClinicalTrials.gov More Intrauterine Device Migration trials