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Abdominal wall anesthetic versus local wound anesthetic in laparoscopic endometriosis surgery; a prospective randomized controlled double-blinded study

Phase 1
Conditions
The study subjects are patients with endometriosis needing surgical treatment.
Therapeutic area: Analytical, Diagnostic and Therapeutic Techniques and Equipment [E] - Anesthesia and Analgesia [E03]
Registration Number
EUCTR2020-004353-80-FI
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Authorised-recruitment may be ongoing or finished
Sex
Female
Target Recruitment
44
Inclusion Criteria

Age 18-50 years.
Diagnosed or suspected peritoneal endometriosis. Laparoscopic surgery indicated.
ASA 1-3.
The study subject is able to understand the study plan and to give informed consent.
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range 44
F.1.3 Elderly (>=65 years) no
F.1.3.1 Number of subjects for this age range

Exclusion Criteria

Sleep-apnea.
ASA > 3.
Other risk factors related to opioid use.
contraindications to opioids or non-steroidal anti-inflammatory drugs.
continuous opioid intake preoperatively.

Study & Design

Study Type
Interventional clinical trial of medicinal product
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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