Chloroprocaine 2% versus prilocaine 1% for plexus anesthesia in outpatient procedures on forearm and hand
Not Applicable
- Conditions
- Pathologies that require surgery on the forearm or hand under plexus anesthesia
- Registration Number
- DRKS00033417
- Lead Sponsor
- BG Klinikum Unfallkrankenhaus Berlin gGmbH
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
Patients (male/female, outpatient) scheduled for axillary plexus anesthesia
- Age: 18 years and older
- ASA I-III
Exclusion Criteria
- General contraindications to plexus anesthesia
- Pregnancy
- Allergy to any of the medications provided for in the study protocol
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Time until the motor and sensory block resolves is a key prerequisite for the ability to be discharged
- Secondary Outcome Measures
Name Time Method • Surgery possible<br>• Time of first onset of pain (NRS)<br>• Maximum pain postoperatively (NRS)<br>• Painkiller requirement (AWR)<br>• Recording of occurring complications<br>• Time of ability to be discharged (PADSS >= 9 points, plexus anesthesia declining)<br>• Questionnaire Quality of recovery (QoR-9)<br>• Follow-up interview after 7 days:<br>• Pain scores of the 6 postoperative days (maximum, average)<br>• Analgesics taken as planned?<br>• Additional analgesics were necessary?