Patients undergoing shoulder surgery Arthroscopy
Conditions
Interventions
Ultrasound guided interscalene brachial plexus block by 20 mL of 0.25% bupivacaine + 1% lidocaine by a 50-
mm 22G nerve block needle 40 minutes before the surgery,general anesthesia with propofol,
fentanyl and rocuronium induction
followed by sevoflurane and remifentanil anesthesia
Active Comparator Procedure/Surgery,Active Comparator Procedure/Surgery
guided interscalene block,general anesthesia
Sponsors
none
Eligibility
Sex/Gender
All
Age
18 Years to 75 Years
Inclusion criteria
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
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
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| oxidative stress intreoperative and postoperative 18 hours thiol–disulfide balance and C-reactive protein | — |
Secondary
| Measure | Time frame |
|---|---|
| pain in postoperative 18 hours visual analgue scale | — |
Contacts
Public ContactMurat Öksüz
Fatih Sultan Mehmet Health Application and Research Center
Outcome results
None listed