Studies with pain rating scales.
W W Downie, P A Leatham, V M Rhind...
https://pubmed.ncbi.nlm.nih.gov/686873Actively Recruiting
Led by Zagazig University · Updated on 2025-05-14
60
Participants Needed
1
Research Sites
4 weeks
Total Duration
Shoulder pain often results from rotator cuff tears and can significantly affect quality of life and delay rehabilitation. This research compares two types of regional anaesthesia blocks to manage postoperative pain after arthroscopic rotator cuff repair surgery. The study aims to evaluate the analgesic effect of a newer ultrasound-guided shoulder anterior capsular block (SHAC) against the combined suprascapular and axillary nerve blocks (SSNB-ANB), which are commonly used and known for effective pain relief but with some drawbacks like motor block and diaphragm issues. The SHAC block targets all nerves supplying the shoulder consistently at two sites, aiming to spare motor function and allow early movement and rehabilitation. The SSNB-ANB block involves separate nerve blocks for the suprascapular and axillary nerves using ultrasound guidance. Both blocks use injections of bupivacaine with dexamethasone as an adjuvant. The study will randomly assign participants to receive either the SHAC block or the combined SSNB-ANB block during arthroscopic rotator cuff repair surgery. Participants will be monitored for postoperative pain using the Numeric Rating Scale at rest and movement at several intervals up to 24 hours after surgery. Researchers will measure total pethidine use in the first 24 hours, time to first request for rescue analgesia, block performance time, patient satisfaction, and any complications over seven days. The study will assess the potential benefits of the SHAC block for adequate pain control and early rehabilitation after shoulder surgery, with follow-up during the first day and up to a week after surgery.
CONDITIONS
Shoulder Anterior Capsular Block for Postoperative Analgesia in Arthroscopic Rotator Cuff Repair Surgery
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Complete this quick 3-step screening to check your eligibility
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Single day of surgery and immediate postoperative period
Participants receive one of two types of nerve blocks to manage pain during and after arthroscopic rotator cuff repair surgery.
1 visit on the day of surgery
Duration - Up to 7 days after surgery
Participants are monitored for pain relief, analgesic use, satisfaction, and any complications following surgery.
Follow-up assessments within 24 hours and at 7 days post-surgery
Total: 1 location
1
Zagazig University Hospitals
Zagazig, Al Sharqia, Egypt, 44519
Actively Recruiting
S
Sherif M. S. Mowafy, MD
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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