Cervical Erector Spinae Block Versus Interscalene Block for Analgesia in Arthroscopic Shoulder Surgery

Cervical Erector Spinae Block Versus Interscalene Block for Analgesia in Arthroscopic Shoulder Surgery :Randomized controlled Study.

Status

Recruiting

Phases

Phase 2

Study type

Interventional

Source

PACTR

Registry ID

PACTR202502729441308

Enrollment

Registered

2025-02-27

Start date

2024-10-15

Completion date

Unknown

Last updated

2026-01-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anaesthesia

Interventions

cervical erectospinae block

interscalene block

controlled group

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: ? Aged between 19 and 70 years ? American Society of Anesthesiologists Classification (ASA) I and II; and scheduled to undergo arthroscopic shoulder surgery under general surgery.

Exclusion criteria

Exclusion criteria: ? allergy to LA ? infection at the puncture site ? bleeding diathesis ? cognitive impairment

Design outcomes

Primary

Measure	Time frame
The analgesic effect will be assessed by postoperative Visual Analogue Scale (VAS )score at 4 hour at rest	—

Secondary

Measure	Time frame
? Intraoperative and postoperative hemodynamics heart rate (HR)(beats/minutes) and mean arterial blood pressure (MAP)(mmHg) ?Postoperative use of analgesia Time to first ask for analgesia Dose of pethidine (mg) Number of patients who will require postoperative analgesia	—

Countries

Egypt

Contacts

Public Contactdr.ahmed Mostafa El shaarawy

assistant professor

drshaarawy@gmail.com01141015584

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Feb 4, 2026