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Enrolling By Invitation NCT06653400

Combined Ketorolac and Lidocaine Paracervical Block for Office Hysteroscopy

Conditions: Abnormal Uterine Bleeding, Analgesia, Paracervical Block

Sex: Female

Ages: 18 Years – N/A

Healthy volunteers: Yes

Phase: PHASE1

Enrollment: 60

Sponsor: Icahn School of Medicine at Mount Sinai

Location: Mount Sinai New York New York

Summary

A randomized double-blind placebo controlled trial comparing the effect of a combined ketorolac and lidocaine paracervical block with a standard lidocaine paracervical block on procedure related pain with office hysteroscopies.

Eligibility Criteria

Inclusion Criteria: * Patients assigned female at birth, * booked for office hysteroscopy at Mount Sinai Hospital faculty practice associates. Exclusion Criteria: * Allergy to ketorolac or non-steroidal anti-inflammatory medications * Allergy to lidocaine * Presence of thrombocytopenia * Contraindications to lidocaine * History of gastritis or gastric ulcer * Acute renal failure or chronic renal disease * Chronic liver disease * History of bleeding diathesis * Long term narcotic use

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View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT06653400). StuddyBuddy aggregates publicly available trial information.