Spinal anaesthesia with chloroprocain versus total intravenous anaesthesia for outpatient knee arthroscopy

Not Applicable

• Conditions: Diseases or conditions that indicate to an outpatient knee arthroscopy; M23; Internal derangement of knee

• Registration Number: DRKS00005989
• Lead Sponsor: Klinik für Anästhesiologie und Operative Intensivmedizin der Universitätsmedizin Mannheim

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2014-04-15
• Study Completion: 2015-08-24
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 50

Inclusion Criteria

1. Patients (male/female) with outpatient knee arthroscopy
2. Age 18-80 years
3. American Society of Anesthesiologists (ASA) physical status I-III

Exclusion Criteria

1. Contraindications for spinal anaesthesia as well as general anaesthesia
2. Allergy to one of the used drugs for spinal- or general-anaesthesia or for
postoperative analgesia

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Duration of stay in the day-surgery centre measured from anaesthesia induction until discharge in minutes.

Secondary Outcome Measures

Name	Time	Method
- first occurrence of pain after anaesthesia induction, measured in minutes<br><br>- Patient’s overall satisfaction and quality of recovery, measured by QoR9-Questionaire and a standardized interview<br><br>- adverse side effects, measured by a standardized telephone-interview 7 days after the operation<br>