EMLA Cream in Hysteroscopy Practice

Status Not yet recruiting

Clinical Trial Summary

The aim of this study is to investigate the efficacy of 5% lidocaine 25 mg-prilocaine 25 mg/g cream (EMLA®) applied to the uterine cervix for reducing pain during diagnostic hysteroscopy, using a visual analogue scale (VAS) for pain, and whether it can replace general anesthesia that may be required for some cases of office hysteroscopy.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Anesthetics, Local

Clinical Trial Details

NCT number	NCT02640183
Study type	Interventional
Source	Ain Shams Maternity Hospital
Contact
Status	Not yet recruiting
Phase	Phase 2
Start date	September 2015
Completion date	March 2016

View Details

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