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A Comparative Study Between Ultrasound Guided Thoracic Paravertebral Block VS Serrartus Anterior Muscle Block in VATS as Regard Their Effectiveness in Post-operative Analgesia

A

Ain Shams University

Status

Enrolling

Conditions

Post Operative Pain, Acute

Treatments

Procedure: thoracic paravertebal block
Procedure: serratus anterior muscle block

Study type

Interventional

Funder types

Other

Identifiers

NCT05971368
paravertebral vs serratus

Details and patient eligibility

About

A comparative study between ultrasound guided thoracic paravertebral block VS ultrasound guided serrartus anterior muscle block in video-assisted thoracoscopic surgeries as regard their effectiveness in post-operative analgesia

Full description

The use of loco-regional analgesia is recommended to control postoperative pain after VATS as it allows opioid sparing and facilitates early postoperative rehabilitation. Different loco-regional analgesic techniques could be used to control pain after thoracic surgery such as a paravertebral block, an intercostal block and serratus plane block. In this study, Thoracic paravertebral nerve block will be compared to Serratus anterior nerve block, both will be done Ultrasound guided (USG) using bupivacaine (0.25%) for postoperative analgesia.

Enrollment

80 estimated patients

Sex

All

Ages

20 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Patients American Society of Anesthesiologists physical status (ASA) I to II
  • Both sexes.
  • Aged ≥ 20 to ≤ 65years.
  • Scheduled for VATS under general anesthesia.

Exclusion criteria

  • Patient's refusal.
  • Patients American Society of Anesthesiologists physical status (ASA) III to IV
  • Patients with major spine deformities.
  • Disruption of the local anatomy, secondary, for instance, to the presence of chest drains or surgical emphysema, resulting in difficulty in ultrasound interpretation and distortion of tissue planes.
  • Patients with bleeding disorders and coagulopathy.
  • Infection at the injection site.
  • Known allergy to local anesthetics.
  • Patients with pre-existing myopathy or neuropathy.
  • Ipsilateral diaphragmatic paresis.
  • Tumors in the paravertebral space at the level of injection.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

80 participants in 2 patient groups

Group A: Patients will receive ultrasound guided thoracic paravertebral block
Active Comparator group
Description:
Group A: Patients will receive ultrasound guided thoraxic paravertebral block with 0.25% bupivacaine 0.4 ml/kg (max. 40 ml and not exceeding toxic dose of bupivacaine 2.5mg/kg) after induction of anesthesia.
Treatment:
Procedure: thoracic paravertebal block
Group B: Patients will receive ultrasound guided serratus anterior muscle block
Active Comparator group
Description:
Group B: Patients will receive ultrasound guided serratus anterior muscle block with 0.25% bupivacaine 0.4 ml/kg (max. 40 ml and not exceeding toxic dose of bupivacaine 2.5mg/kg) after induction of anesthesia.
Treatment:
Procedure: serratus anterior muscle block

Trial contacts and locations

1

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Central trial contact

aya gamal abdelhamid, MSC

Data sourced from clinicaltrials.gov

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