Rupture of rotator cuff tendon. Rotator cuff tear or rupture, not specified as traumatic
Conditions
Interventions
Intervention 1: Intervention group (first group): the Intervention patient will be given medications to help relieve symptoms on the first 24 hours after surgery. So, pain control pump will be given (
if the pain score is greater than or equal to 4.). Control patients will be blinded to the injection of placebo pain control pump (IV PCA) with the same volume and appearance as group 1, containing no
Sponsors
Shiraz University of Medical Sciences
Eligibility
Sex/Gender
All
Age
30 Years to 70 Years
Inclusion criteria
Inclusion criteria: Adult patients with ASA grade I or II (American Society of Anesthesiology classification) patients between 30 and 70 years old Patients who candidate for rotator cuff surgery
Exclusion criteria
Exclusion criteria: Allergy to the drugs used in the study Positive history of chemotherapy and radiotherapy Positive history of liver, kidney, hormone problems, central nervous system disorders and diseases, depression and anxiety Addiction to drugs, alcohol and smoking Use of Corticosteroid and Benzodiazepine pregnancy
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain. Timepoint: Every 10 minutes during recovery, 6 hours, 12 hours, 24 hours, 48 hours, one week, ten days and two weeks after the end of the intervention. Method of measurement: Questionnaire and Numerical Pain Rating Scale (NRS). | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMahshid Hashemi nasab
Shiraz University of Medical Sciences
Outcome results
None listed