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Clinical Trials/IRCT20140427017455N5
IRCT20140427017455N5CompletedPhase 3

Comparison of the efficacy of different doses of adjuvant perineural tramadol to 0.25% bupivacaine in prolongation of postoperative analgesia in arthroscopic shoulder surgeries under interscalene block

Tehran University of Medical Sciences0 sites60 target enrollmentStarted: TBDLast updated:

Trial Snapshot

Phase
Phase 3
Status
Completed
Enrollment
60

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
18 years to no limit (—)
Sex
All

Inclusion Criteria

  • Patients candidate for Shoulder arthroscopic surgery
  • Age 18 years or more
  • ASA class I-II
  • Intact cognition and contiousness

Exclusion Criteria

  • Patient refusal
  • Contraindication for drug infiltration
  • History of Allergic reactions to drug used in this study
  • Contraindication for intrscalene block
  • Contraindication for tramadol administration
  • Opioid abuse history
  • Pregnancy or baby breast feeding
  • Chronic pain syndromes
  • Any neurological problem in the same side upper limb
  • History of epilepsy
  • Body mass index 40 or higher

Investigators

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