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Ultrasound Guided Block for Postoperative Analgesia in Arthroscopic Shoulder Surgery

M

Menoufia University

Status

Active, not recruiting

Conditions

Analgesia

Treatments

Procedure: Shoulder Block
Procedure: High Thoracic Erector Spinae Plane Block

Study type

Interventional

Funder types

Other

Identifiers

NCT06202430
122023ANET14

Details and patient eligibility

About

This study aimed to compare the efficacy of high thoracic-ESPB with shoulder block as analgesic options for arthroscopic shoulder surgery.

Primary outcome:

• 24-hour analgesic consumption.

Secondary outcomes:

  • Postoperative pain evaluated by: Visual Analogue Pain Scale (VAS).
  • Time to first rescue analgesia and total postoperative consumption of analgesia.
  • Effect of the block on Hemodynamics.
  • Adverse effects in the form of postoperative nausea and vomiting (PONV).
  • Patient satisfaction.

Enrollment

36 patients

Sex

All

Ages

21 to 70 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • All patients within the age range ≥ 21 to ≤ 70 years old.
  • Body mass index (BMI) ≤ 35kg m2.
  • ASA I, II of both sex

Exclusion criteria

  • Refusal of the patient to the study.
  • Infection at the site of injection.
  • Previous known allergy to any drug used in the study by history.
  • Renal disease [Creatinine. >3mg/dl.].
  • Hepatic disease. [ALT>50U/L, AST >50U/L].
  • Un cooperative or psychological unstable patients.
  • Coagulopathy or anticoagulant therapy.
  • Pregnancy.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

36 participants in 2 patient groups

Ultrasound Guided High Thoracic Erector Spinae Plane Block
Active Comparator group
Description:
High Thoracic-ESPB The patient was placed in the lateral decubitus. Subsequently, an ultrasound (US)-guided aseptic technique, with a high-frequency linear probe enveloped in a sterile sheath containing a thin film of US gel, was used to locate the transverse process of T2. After LA skin infiltration, a 22-G block was inserted in a cephalocaudal direction until the space between the fascia of the erector spinae and the transverse process of T2 was identified. After negative aspiration, hydro dissection using 2 mL of saline was performed. Eventually, 30 mL of the LA bupivacaine 0.25% and epinephrine 5 µg/ mL was injected.
Treatment:
Procedure: High Thoracic Erector Spinae Plane Block
Ultrasound Guided Shoulder Block
Active Comparator group
Description:
Shoulder Block Suprascapular nerve block (SSNB) approach: A high-frequency linear probe was utilized across the supra-spinous fossa parallel to the spine of the scapula after skin cleaning with an antiseptic solution, if a deep block is required, a low frequency probe was required. A hyperechoic line was identified, followed by an acoustic shadow that corresponds to the floor of the supra-spinous fossa. The needle was progressed in plane from medial to lateral after local infiltration of the skin with 1% lidocaine. We directed the needle towards the lateral side of the supra-spinous fossa if the neuro-vascular bundle was not evident. After careful aspiration, 10 ml of 0.5% bupivacaine was injected under the supraspinatus muscle. Along with Axillary nerve block technique.
Treatment:
Procedure: Shoulder Block

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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