Clinical Trials Directory

Trials / Not Yet Recruiting

Not Yet RecruitingNCT06767085

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

Pain Management With Lidocaine-prilocaine Spray During Diagnostic Office Hysteroscopy in Postmenopausal Women: a Randomized Controlled Study

Status
Not Yet Recruiting
Phase
Phase 4
Study type
Interventional
Enrollment
106 (estimated)
Sponsor
Cairo University · Academic / Other
Sex
Female
Age
Healthy volunteers
Not accepted

Summary

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

Detailed description

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

Conditions

Interventions

TypeNameDescription
DRUGLidocaine-Prilocaine Topicallidocaine-prilocaine spray on the cervix and cervical canal 5-7 minutes prior to the procedure
DRUGSaline spraysaline spray on the cervix and cervical canal 5-7 minutes prior to the procedure

Timeline

Start date
2025-02-05
Primary completion
2025-07-05
Completion
2025-07-25
First posted
2025-01-09
Last updated
2025-01-09

Source: ClinicalTrials.gov record NCT06767085. Inclusion in this directory is not an endorsement.

Pain Management During Diagnostic Office Hysteroscopy in Postmenopausal Women: a Randomized Study (NCT06767085) · Clinical Trials Directory