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Effect of buprenorphine on pain intensity after surgery

Phase 3
Conditions
Post-operative pain.
Chronic post-thoracotomy pain
G89.22
Registration Number
IRCT20201026049147N1
Lead Sponsor
Mazandaran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
78
Inclusion Criteria

Patient candidate for elective discectomy with 1 or 2 lumbar discs
With ASA class I and II
Age range 35-70
Conscious consent to participate in the study
Hypersensitivity to buprenorphine
Confirmation of diagnosis by physical examination, CT scan and MRI
Patient's willingness to participate in the study and obtaining informed consent

Exclusion Criteria

Patient's unwillingness at any time to continue the study
Incidence of any uncommon side effects during surgery.
Alcohol or drug abuse
Opioids use 24 hours prior to intervention
Involvement of more than two lumbar disc

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Opium usage. Timepoint: 0, 2, 4, 6, 12, 24 hours after surgery. Method of measurement: Checklist.
Secondary Outcome Measures
NameTimeMethod
Pain severity. Timepoint: 0, 2, 4, 6, 12, 24 hours after surery. Method of measurement: Visual analogue scale.
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