Shoulder Arthroscopy Clinical Trial
Official title:
Comparison Between Ultrasound Guided Pericapsular Nerve Group (PENG) Block and Interscalene Brachial Plexus Block for Postoperative Analgesia Following Shoulder Arthroscopy: Prospective, Randomized Controlled Trial
The study aimed to compare ultrasound guided pericapsular nerve group (PENG) block versus interscalene brachial plexus block for postoperative analgesia following shoulder arthroscopy.
Status | Recruiting |
Enrollment | 50 |
Est. completion date | December 1, 2024 |
Est. primary completion date | December 1, 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 60 Years |
Eligibility | Inclusion Criteria: - Age from 18 to 60 years old. - Both genders. - BMI =35 kg/m2. - American Society of Anesthesiologists Physical Status (ASA-PS) Class I and II. - Patient who will be scheduled for an elective unilateral arthroscopic shoulder surgery. Exclusion Criteria: - Refusal of procedure or participation in the study - Patient under age of 18 years old or above 60 years' old - Physical status: ASA-PS III or above. - Pregnancy or lactation. - Infection at site of injection. - Psychiatric illness. - CNS Diseases like (epilepsy, stroke …etc.) or neurological disease affecting patient's upper limb. - Evidence of coagulopathy or anticoagulation. - Patients with respiratory disease, renal or hepatic insufficiency. - infection of the skin in the puncture area. - Allergy against any of the drugs to be used. - Obesity (BMI >35 kg/m2). |
Country | Name | City | State |
---|---|---|---|
Egypt | Ain Shams University | Cairo |
Lead Sponsor | Collaborator |
---|---|
Ain Shams University |
Egypt,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | First time for requiring analgesia | First time for requiring analgesia. It will be defined as the time from recovery until VAS score greater than 3. | 24 hours postoperatively | |
Secondary | Total amount of pethidine consumption in the first 24 hours | If the patient complained of pain, intravenous pethidine sulfate will be (50mg/dose) to be repeated on demand (VAS is > 3) provided that the total 24-hour dosage not to exceed 50 mg every 6 hours. | 24 hours postoperatively | |
Secondary | The degree of pain | The degree of pain will be measured using visual analogue scale (VAS)ranging from 0 to 10, where 0 no pain and 10 maximum pain. It will be evaluated on arrival to PACU (T0) then at 2, 4, 6, 12, and 24 h postoperatively. | 24 hours postoperatively | |
Secondary | Complications | Any complications during and after the performance of the block - for example, pneumothorax, Horner's syndrome, hoarseness of voice, difficulty in breathing, weakness, and paresthesia in the arm will be recorded. | 24 hours postoperatively |
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