Comparisson of two epidural drugs in day-case surgery

Phase 1

• Conditions: Patients scheduled for ambulatory knee arthroscopy surgery receive one of the two spinal anaesthetics; Therapeutic area: Analytical, Diagnostic and Therapeutic Techniques and Equipment [E] - Anesthesia and Analgesia [E03]

• Registration Number: EUCTR2015-001944-13-NL
• Lead Sponsor: Zaans Medisch Centrum

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2016-02-29
• Last Update Posted: 20 August 2018

Recruitment & Eligibility

• Status: ot Recruiting
• Sex: All
• Target Recruitment: 175

Inclusion Criteria

-Scheduled ambulatory knee arthroscopy
-Age = 18 years
-ASA physical status I- II

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 175
F.1.3 Elderly (>=65 years) no
F.1.3.1 Number of subjects for this age range

Exclusion Criteria

-Allergy to one of the study drugs
-Contraindication to neuraxial anaesthesia
-Previous neuropathy to the lower extremities
-Pregnancy

Study & Design

• Study Type: Interventional clinical trial of medicinal product
• Study Design: Not specified