Dosage finding for spinal anaesthesia using chloroprocaine 1% in patients undergoing perianal outpatient surgery.

Not Applicable

• Conditions: K62; Other diseases of anus and rectum

• Registration Number: DRKS00007121
• Lead Sponsor: Klinik für Anästhesiologie und Operative Intensivmedizin der Universitätsmedizin Mannheim

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2014-10-30
• Study Completion: 2015-09-23
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 120

Inclusion Criteria

Diseases of anus or rectum, that make an operative intervention in an ambulatory setting necessary.

Exclusion Criteria

Contraindications against spinal anesthesia. Allergies against local anesthetics or against the postoperative used analgetics.

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Duration of stay in the day-surgery centre (from induction of anesthesia to readiness for home discharge in minutes)

Secondary Outcome Measures

Name	Time	Method
- Expansion of sensory and motor block (modified bromage score, insensitive dermatomes (pinprick) counted upwards from S5)<br>- time from induction of anesthesia to unassisted ambulation in minutes<br>- time from induction of anesthesia first spontaneous micturition in minutes<br>- time from induction of anesthesia to first occurence of pain in minutes<br>- postoperative demand of analgesics<br>- incidence of adverse side effects