Serratus Anterior Plane Block Versus Pericapsular Nerve Group Block for Shoulder Surgery
Ultrasound-guided Serratus Anterior Plane Block Versus Pericapsular Nerve Group Block (PENG) for Postoperative Analgesia in in Arthroscopic Shoulder Surgery: a Randomized Controlled Trial
1 other identifier
interventional
50
1 country
1
Brief Summary
Effective analgesia in arthroscopic shoulder surgery is a major concern and is essential for all aspects of the patient's recovery. The aim of this study is to assess the quality of pain relief in patients who will undergo arthroscopic shoulder surgeries receiving either serratus anterior plane block versus PENG block comparing and evaluating the differences between the two techniques.It is hypothesized that PENG block will be comparable to serratus anterior plane block as a promising effective alternative for analgesia for arthroscopic shoulder surgeries with fewer side effects. It is suggested that the PENG block can be safely applied for analgesia.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started May 2023
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
March 6, 2023
CompletedFirst Posted
Study publicly available on registry
March 16, 2023
CompletedStudy Start
First participant enrolled
May 21, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 15, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
March 10, 2024
CompletedMay 30, 2025
May 1, 2025
9 months
March 6, 2023
May 25, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Visual analogue score (VAS) for pain assessment at 6 hour postoperative
VAS score from 0 to 10 (0 = no pain and 10 = the worst imaginable pain) will be assessed 6 hour after the procedure.
at 6 hour after the procedure
Secondary Outcomes (6)
First analgesic request
Up to 24 hours after the procedure
Total analgesic requirements of fentanyl
Up to 24 hours after the procedure
Visual analogue score (VAS) for pain assessment
Up to 24 hours after the procedure
Heart rate (HR)
During the procedure
Mean arterial blood pressure (MAP)
During the procedure
- +1 more secondary outcomes
Study Arms (2)
Group A (SAPB)
ACTIVE COMPARATORUltrasound-guided SAPB will be applied while the patient is in the supine position.
Group B (PENG block)
ACTIVE COMPARATORUltrasound-guided PENG block will be performed under strict aseptic precautions and patient's arm will be placed in external rotation and abducted at 45 degrees
Interventions
The latissimus dorsi muscle between the midaxillary line and the posterior axillary line will be located under ultrasound guidance. The needle will be inserted into the plane from top to bottom until the serratus anterior surface, and the injectate will be slowly administered.
Ultrasound-guided PENG block will be performed under strict aseptic precautions and patient's arm will be placed in external rotation and abducted at 45 degrees. A linear ultrasound probe will be placed longitudinally between the coracoid and the humeral head. After defining the humeral head, the tendon of the subscapular muscle and the deltoid muscle over it, the needle will be inserted using the "in plane" technique. When the needle will have passed through the deltoid muscle and touched the subscapularis tendon, a bone-like hard tissue will be felt and the needle could not be advanced further. The needle tip will be placed Between the deltoid muscle and subscapularis tendon, and the injectate will be slowly administered.
Eligibility Criteria
You may qualify if:
- American Society of Anesthesiology (ASA) 1 or 2 patients.
- Scheduled for elective unilateral shoulder arthroscopy.
You may not qualify if:
- Patient's refusal.
- Altered mental status or un-cooperative patients.
- History of known sensitivity to the used anesthetics.
- Bleeding or coagulation diathesis.
- Infection or redness at the injection site.
- Significant cardiac dysfunction, hepatic, or renal impairment.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Mansoura University
Al Mansurah, 35511, Egypt
Related Publications (7)
Casas Reza P, Dieguez Garcia P, Gestal Vazquez M, Sampayo Rodriguez L, Lopez Alvarez S. Pericapsular nerve group block for hip surgery. Minerva Anestesiol. 2020 Apr;86(4):463-465. doi: 10.23736/S0375-9393.20.14166-X. Epub 2020 Jan 28. No abstract available.
PMID: 32000476BACKGROUNDvan Erp JHJ, Ostendorf M, Lansdaal JR. Shoulder surgery in beach chair position causing perioperative stroke: Four cases and a review of the literature. J Orthop. 2019 May 27;16(6):493-495. doi: 10.1016/j.jor.2019.05.009. eCollection 2019 Nov-Dec.
PMID: 31680738BACKGROUNDKapukaya F, Ekinci M, Ciftci B, Atalay YO, Golboyu BE, Kuyucu E, Demiraran Y. Erector spinae plane block vs interscalene brachial plexus block for postoperative analgesia management in patients who underwent shoulder arthroscopy. BMC Anesthesiol. 2022 May 12;22(1):142. doi: 10.1186/s12871-022-01687-5.
PMID: 35550031BACKGROUNDKupeli I, Yazici Kara M. Anesthesia or analgesia? New block for shoulder surgery: pericapsular nerve group block. Braz J Anesthesiol. 2022 Sep-Oct;72(5):669-672. doi: 10.1016/j.bjane.2021.05.009. Epub 2021 Jun 9.
PMID: 34118263BACKGROUNDPatel MS, Abboud JA, Sethi PM. Perioperative pain management for shoulder surgery: evolving techniques. J Shoulder Elbow Surg. 2020 Nov;29(11):e416-e433. doi: 10.1016/j.jse.2020.04.049. Epub 2020 Jun 9.
PMID: 32844751BACKGROUNDSripada R, Bowens C Jr. Regional anesthesia procedures for shoulder and upper arm surgery upper extremity update--2005 to present. Int Anesthesiol Clin. 2012 Winter;50(1):26-46. doi: 10.1097/AIA.0b013e31821a0284.
PMID: 22227421BACKGROUNDZhu H, Zhang C, Yan C. The Anesthetic Effect of Ultrasound-Guided Serratus Anterior Plane Block in Arthroscopic Shoulder Surgery and Its Effect on Postoperative Analgesia. J Healthc Eng. 2022 Mar 15;2022:8968805. doi: 10.1155/2022/8968805. eCollection 2022.
PMID: 35356610BACKGROUND
Study Officials
- PRINCIPAL INVESTIGATOR
EL-Deeb
Faculty of Medicine, Mansoura University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, OUTCOMES ASSESSOR
- Masking Details
- The study subjects and the resident assessing the outcomes will be blinded to the study group. A single investigator will assess the patients for eligibility, obtain written informed consent, open the sealed opaque envelopes containing group allocation, perform the block, and administer bupivacaine solution.
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Lecturer of anesthesia, ICU & pain management; Faculty of Medicine
Study Record Dates
First Submitted
March 6, 2023
First Posted
March 16, 2023
Study Start
May 21, 2023
Primary Completion
February 15, 2024
Study Completion
March 10, 2024
Last Updated
May 30, 2025
Record last verified: 2025-05
Data Sharing
- IPD Sharing
- Will not share