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Clinical Trials/IRCT20201026049147N1
IRCT20201026049147N1
Completed
Phase 3

Evaluating the effect of preoperative sublingual buprenorphine on pain intensity after lumbar disc surgery

Mazandaran University of Medical Sciences0 sites78 target enrollmentTBD
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ConditionsPost-operative pain.Chronic post-thoracotomy painG89.22

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Post-operative pain.
Sponsor
Mazandaran University of Medical Sciences
Enrollment
78
Status
Completed
Last Updated
5 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
5 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

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

Outcomes

Primary Outcomes

Not specified

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