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RecruitingNCT05739201Updated Sep 6, 2023

ISB, SSNB, and PENG Block for Arthroscopic Shoulder Surgery

An interventional study of interscalene nerve block and anterior suprascapular nerve block in Interscalene Nerve Block, Anterior Suprascapular Nerve Block and Arthroscopic Shoulder Surgery, sponsored by Tanta University. Recruiting at 1 site in Egypt. Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2023-09-06.

Sponsored by Tanta University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Dec 2023, 2 years 9 months ago, but the record still lists the study as recruiting.
  • Started Feb 2023; still recruiting 3 years 7 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
90
Allocation
Randomized
Ages
18 Years to 65 Years
Sex
All
01

Study summary

This study is designed to investigate the post-operative analgesic effect of interscalene nerve block or anterior suprascapular nerve block compared to pericapsular nerve group block in patient undergoing elective arthroscopic shoulder surgery.

Read the detailed description

Shoulder arthroscopy is a common outpatient operation with an increasing number of indications and complexity. Early postoperative pain immediately following shoulder surgery is a major concern and cause of distress for patients and orthopedic surgeons. Adequate pain control is vital for all aspects of the patient's recovery.

Nowadays, several ultrasound -guided regional anesthesia methods are used for postoperative analgesia. Regional techniques such as interscalene and supraclavicular blocks are usually preferred for shoulder analgesia. Interscalene brachial plexus block (ISB) is the gold standard technique in this area.

Suprascapular nerve block (SSB) has been proposed as an alternative to the ISB in providing analgesia for shoulder surgeries as it has a lower likelihood of causing phrenic nerve blockade.

The pericapsular nerve group (PENG) block has been suggested to be safely applied for analgesia and can be part of surgical anesthesia, but alone is not sufficient for anesthesia in shoulder surgery. The block of this area did not cause motor block or pulmonary complications, nor result in muscle laxity, blocking only the shoulder and the upper third of the humerus.

02

Conditions studied

  • Interscalene Nerve Block
  • Anterior Suprascapular Nerve Block
  • Arthroscopic Shoulder Surgery
03

In context

Lead sponsor

Tanta University is the lead sponsor of 963 studies on the registry; 304 are open to participants now.

Of its 16 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Adult patients.
  • ASA class I and II and scheduled for elective shoulder arthroscopy.

Exclusion criteria

Exclusion Criteria:

  • Patient who refuses the regional anesthesia technique.
  • History of allergy to local anesthetics.
  • Local infection at the site of the block.
  • History of Pre-existing major organ dysfunction such as hepatic and renal failure.
  • History of pre-existing lung disease (COPD, uncontrolled asthma).
  • Preexisting upper extremity neurological abnormality or neuropathy.
  • Difficulties in comprehending (NRS).
  • Chronic opioid users (opioid intake more than 3 months).
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Triple (Participant, Care provider, Investigator)
Enrollment
90 participants (estimated)

Study arms

  • Active comparator
    Group (I)

    30 patients will receive interscalene nerve block.

    Procedure: interscalene nerve block

  • Active comparator
    Group (II)

    30 Patients will receive anterior suprascapular nerve block.

    Procedure: anterior suprascapular nerve block

  • Active comparator
    Group (III)

    30 atients will receive pericapsular nerve group block around shoulder surgery

    Procedure: Peri-capsular nerve group block

Interventions

  • Procedureinterscalene nerve block

    Patients will receive interscalene nerve block, in which the patient will be in supine position with the head turned to the contralateral side using an ultrasound scan to identify the C5 and C6 nerve roots between the scalene muscles.15 ml of 0.25% Bupivacaine will be deposited between the C5 and C6 nerve roots, within the interscalene groove using a 22 gauge-regional block needle.

  • Procedureanterior suprascapular nerve block

    Patients will receive anterior suprascapular nerve block, in which the patient will be in supine position with the head turned to the contralateral side, using an ultrasound the nerve will be traced as it diverges from the brachial plexus to lie under the omohyoid muscle in the supraclavicular fossa. 15 ml of 0.25% Bupivacaine will be deposited lateral to the suprascapular nerve, underneath the omohyoid muscle using a 22 gauge-regional block needle.

  • ProcedurePeri-capsular nerve group block

    Patients will receive PENG block, in which the patient will be in supine position and the patient's arm will be placed in external rotation and abducted at 45 degrees, using an ultrasound the humeral head, the tendon of the subscapularis muscle and the deltoid muscle over it will be defined, 15 ml of 0.25% Bupivacaine will be placed between the deltoid muscle and subscapularis tendon using a 22 gauge-regional block needle.

06

What researchers measure

Primary outcomes

  1. the total opioid consumption.

    Postoperative analgesia will be assessed by total opioid consumption and time till administration of first rescue analgesia will be recorded.

    Time frame: 24-hour postoperatively

07

Study locations

1 of 1 sites recruiting
  • Shrouk Mohamed Elsawaf
    Tanta, EL-Gharbia 31527, Egypt
    Recruiting
08

References and documents

Individual participant data

Plan to share: Yes — The data will be available upon reasonable request from the principal investigator

Supporting information: Study protocol, Sap

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 6, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05739201
Lead sponsor
Tanta University
Responsible party
Shrouk Elsawaf (Resident, Tanta University) — Principal investigator
First posted
Feb 22, 2023
Start date
Feb 20, 2023
Primary completion
Dec 20, 2023 (estimated)
Completion
Dec 20, 2023 (estimated)
Last update
Sep 6, 2023

Study contacts

Shrouk M Elsawaf, Master
Contact
Shroukms95@gmail.com
+201091533902 ext. +20
Ayman A Youssef, MD
principal investigator · Professor of Anaesthesiology, Surgical Intensive Care and Pain Therapy, Faculty of Medicine, Tanta University, Egypt

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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