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NCT02640183

Lidocaine-Prilocaine (EMLA®) Cream in Hysteroscopy Practice: A Prospective Randomized Non-blinded Controlled Study

Status unknown Phase 2 Last updated 22 December 2015
What this trial tests

Phase 2 trial testing EMLA in Anesthetics, Local in 184 participants. Status unknown.

Timeline
1 September 2015
Primary endpoint
1 March 2016
1 March 2016

Quick facts

Lead sponsorAin Shams Maternity Hospital
PhasePhase 2
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment184
Start date1 September 2015
Primary completion1 March 2016
Estimated completion1 March 2016

Drugs / interventions tested

Conditions studied

Sponsor

Ain Shams Maternity Hospital

Who can join

18 and older, female only, with Anesthetics, Local. Patients with the condition only — healthy volunteers not accepted.

What's being measured

Primary outcomes are the specific endpoints the trial is designed to prove or disprove.

Sponsor's own description

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.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Pain relief for outpatient hysteroscopy.
    Ahmad G, Saluja S, O'Flynn H, Sorrentino A, et al · · 2017 · cited 34× · PMID 35611933 · DOI 10.1002/14651858.cd007710.pub3

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Other trials of EMLA

Trials testing the same drug.

Other Ain Shams Maternity Hospital trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT02640183.

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