Topical EMLA-patch for postoperative wound pain after gynecological laparoscopy

Topical EMLA-patch for postoperative wound pain after gynecological laparoscopy - EMGYN

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

DRKS

Registry ID

DRKS00003869

Enrollment

120

Registered

2012-05-04

Start date

2012-05-15

Completion date

Unknown

Last updated

2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Other gynaecologic diseases in which a laparoscopy has to be performed. D25.9 R10.3

Interventions

Group 1: Study collective: EMLA-patch Group 2: Control collective: placebo (conventional patch)

Eligibility

Sex/Gender

Female

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: patients with laparoscopy

Exclusion criteria

Exclusion criteria: allergy against amide-anesthetics

Design outcomes

Primary

Measure	Time frame
Priniciple aim of this study is postoperative pain using EMLA-patches compared to conventional patches (controlled by the standardized Questionaire"Short form Mc Gill Pain Questionaire").	—

Secondary

Measure	Time frame
Further study endpoints are length of hospital stay and need of additional medication for pain relief.	—

Countries

Germany

Contacts

Public ContactAmadeus Hornemann

Universitätsklinikum Mannheim

amadeus.hornemann@umm.de+49/621-383-5188

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026