Het effect van adrenaline toegevoegd aan het verdovingsmiddel, op de werkingsduur van de voetverdoving.

Completed

• Conditions: Patients scheduled for continuous popliteal sciatic nerve block for talocrural arthrodesis; subtalar fusion or Lisfranc arthrodesis at the Sint Maartenskliniek

• Registration Number: NL-OMON23190
• Lead Sponsor: Sint Maartenskliniek Nijmegen

Brief Summary

/A

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 28 February 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 30

Inclusion Criteria

1. Patients of 18 years or older;

2. ASA physical status classification I – III;

Exclusion Criteria

1. Contra-indications for regional anesthesia;

2. Known hypersensitivity to amide-type local anesthetics;

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Duration of postoperative analgesia depicted in Time To First Request: time between t = 0 and time of first request for postoperative analgesia (PCA ropivacaine 0.2% through popliteal catheter).

Secondary Outcome Measures

Name	Time	Method
1. Onset of sensory and motor block;<br /><br>2. Numeric Rating pain Scores (NRS 0-10) at rest and during movement directly postoperative, at t = 24h and if necessary at t = 48h;<br /><br>3. Satisfaction (NRS 0-10) with anesthetic technique.