Pain Management During Diagnostic Office Hysteroscopy in Postmenopausal Women: a Randomized Study

NCT06767085 Status: NOT_YET_RECRUITING Phase: PHASE4 Type: INTERVENTIONAL Enrollment: 106

Last updated 2025-01-09

No results posted yet for this study

Summary

To assess the effectiveness of lidocaine-prilocaine spray versus placebo in minimizing the pain experienced by postmenopausal patients during diagnostic of铿乧e hysteroscopy and to assess the ease of insertion of hysteroscope as reported by the hysteroscopists

Conditions

  • Office Hysteroscopy

Interventions

DRUG

Lidocaine-Prilocaine Topical

lidocaine-prilocaine spray on the cervix and cervical canal 5-7 minutes prior to the procedure

DRUG

Saline spray

saline spray on the cervix and cervical canal 5-7 minutes prior to the procedure

Sponsors & Collaborators

  • Cairo University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-02-05
Primary Completion
2025-07-05
Completion
2025-07-25

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06767085 on ClinicalTrials.gov