Status:
COMPLETED
Added Value of Local Clonidine for Spine Postoperative Pain Control, in Addition to Bupivacaine
Lead Sponsor:
St Joseph University, Beirut, Lebanon
Conditions:
Post-operative Pain
Eligibility:
All Genders
18-72 years
Phase:
PHASE4
Brief Summary
The objective of this prospective randomized double-blind study is to evaluate the added analgesic value of clonidine to the conventional local bupivacaine wound infiltration in posterior spine surger...
Detailed Description
Patients candidates to posterior spine surgery (Micro-discectomy, Lumbar laminectomy with or without fusion, cervical laminectomy) are asked to participate to this prospective study. After verificatio...
Eligibility Criteria
Inclusion
- First (not recurrent) posterior spinal surgery at the operated site
- American Society of Anesthesiologists class I or II (operative risk)
Exclusion
- Allergy to local anesthetics or to clonidine
- Pregnancy
- Raynaud's syndrome
- Thromboangiitis obliterans
- History of substance abuse
- Current treatment with corticosteroids
Key Trial Info
Start Date :
January 1 2013
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
December 1 2015
Estimated Enrollment :
225 Patients enrolled
Trial Details
Trial ID
NCT01902108
Start Date
January 1 2013
End Date
December 1 2015
Last Update
December 8 2015
Active Locations (1)
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1
Hotel Dieu de france Hospital
Beirut, Lebanon, 16-6830