Clonidine as Additive for Locoregional Postoperative Analgesia inFoot and Anckle Surgery

• Conditions: Postoperative pain; Therapeutic area: Analytical, Diagnostic and Therapeutic Techniques and Equipment [E] - Anesthesia and Analgesia [E03]

• Registration Number: EUCTR2014-004964-39-NL
• Lead Sponsor: Sint Antonius Ziekenhuis

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2015-05-21
• Last Update Posted: 10 July 2015

Recruitment & Eligibility

• Status: Authorised-recruitment may be ongoing or finished
• Sex: All
• Target Recruitment: Not specified

Inclusion Criteria

Patients above 18 years of age who undergo foot/anckle surgery
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range 120
F.1.3 Elderly (>=65 years) no
F.1.3.1 Number of subjects for this age range

Exclusion Criteria

Neuropathy, chronic pain and allergy to substance used.

Study & Design

• Study Type: Interventional clinical trial of medicinal product
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Main Objective: Duration of loco-regional anesthesia ;Secondary Objective: Postoperative pain, patient satisfaction;Primary end point(s): Duration of block; postoperative pain;Timepoint(s) of evaluation of this end point: Painscores mmediately after surgery and at 18.00 and 21.00 on the day of surgery. At 8.00 on the 1st postoperative day.

Secondary Outcome Measures

Name	Time	Method
Secondary end point(s): Patient satisfaction; nausea; hypotension; sedation;Timepoint(s) of evaluation of this end point: mmediately after surgery and at 18.00 and 21.00 on the day of surgery. At 8.00 on the 1st postoperative day.