Clonidine as Additive for Locoregional Postoperative Analgesia in Foot and Anckle Surgery

Completed

• Conditions: Postoperative pain; extension of postoperative analgesia; 10009720

• Registration Number: NL-OMON42282
• Lead Sponsor: Sint Antonius Ziekenhuis

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 23 April 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 120

Inclusion Criteria

Patients for elective foot/anckle surgery

Exclusion Criteria

Neuropathy; chronic pain

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>FAR = first analgesic request. The duration of popliteal block till the time of<br /><br>first analgesic request on the ward.</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Painscores at 18.00 and 21.00 on the day of surgery and painscores at 08.00 on<br /><br>the postoperative day.<br /><br>Sedation, hypotension and nausea are also documented.</p><br>