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Evaluation of the effects of general anesthesia and ultrasonography-guided interscalene block on pain and oxidative stress using thiolâ€disulfide balance and C-reactive protein levels: a randomized trial

Not Applicable
Completed
Conditions
Patients undergoing shoulder surgery
Arthroscopy
Brachial plexus block
C&#45
Reactive protein
General anesthesia
Pain
Sulfhydril compounds.
Registration Number
TCTR20200329001
Lead Sponsor
none
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
42
Inclusion Criteria

patients scheduled to undergo shoulder arthroscopy were those who presented to the Orthopedics and Traumatology Outpatient Clinics of our hospital with a complaint of shoulder pain and who remained unresponsive to conservative therapies after being diagnosed with subacromial impingement syndrome.

Exclusion Criteria

; those allergic to the medications used in the present study; those who were obese (body mass index [BMI] > 35 kg/m2); those with an infection at the injection site; those who underwent surgical intervention or had anatomical deformation at the relevant site; those receiving antithrombotic therapy and thus having changes in coagulation parameters; those with severe pulmonary disease, phrenic nerve palsy, diaphragm paralysis, pneumothorax, or neurological dysfunction in upper extremities; those who have received or are currently receiving psychiatric therapy; those receiving opioid therapy for a long period; those with known alcohol and/or drug addiction; those with diabetes mellitus, rheumatoid arthritis, chronic kidney failure, liver diseases, cardiac insufficiency, or Alzheimer’s disease; oncology patients; those who did not accept the relevant anesthesia method after randomization; and those with pathologies such as labral lesions, recurrent instability, or rotator cuff rupture requiring arthroscopic procedure in addition to subacromial decompression

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
oxidative stress intreoperative and postoperative 18 hours thiolâ€disulfide balance and C-reactive protein
Secondary Outcome Measures
NameTimeMethod
pain in postoperative 18 hours visual analgue scale
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