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Ultrasound-Guided Mid-Point Transverse Process to Pleura Block for Thoracotomy Incisions

T

Tanta University

Status

Unknown

Conditions

Postoperative Pain
Thoracotomy
Pre-emptive

Treatments

Procedure: Sham group
Procedure: Midpoint transverse process block group

Study type

Interventional

Funder types

Other

Identifiers

NCT05044858
34646/4/21

Details and patient eligibility

About

This study is designed to investigate the analgesic efficacy of pre-emptive ultrasound-guided midpoint transverse process to pleura (MTP) block for posterolateral thoracotomy in cardiothoracic surgeries.

Full description

Preemptive preoperative analgesia was first proposed, over the years it has been gradually regarded as an intervention given before incision, facilitating mobilization and functional rehabilitation after surgery, reducing postoperative opioid consumption, decreasing the incidence of adverse events and improving patient satisfaction.

The Mid Transverse Process to Pleura block, described by Costach et al. involves deposition of drug midway between the transverse process and pleura. Costach et al. postulated that the local anesthetic deposited at this point may reach the paravertebral space through several possible mechanisms, such as spread medially through the gap between the superior costotransverse ligament (SCTL) and vertebral bodies, through fenestrations in SCTL, and laterally through the internal intercostal membrane

Enrollment

70 estimated patients

Sex

All

Ages

21 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients aged 21- and65 years old
  • American Society of Anesthesiologists (ASA) II-III
  • Scheduled for posterolateral thoracotomy operation under general anesthesia

Exclusion criteria

  • Patients with bleeding disorders,
  • Mental or cognitive dysfunction
  • History of chronic analgesic or drug abuse
  • Allergy to local anesthetics
  • Local infection at site of block

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

70 participants in 2 patient groups

Midpoint transverse process block group
Experimental group
Description:
Patients will receive midpoint transverse process block after induction of general anesthesia and before surgical incision
Treatment:
Procedure: Midpoint transverse process block group
Sham group
Sham Comparator group
Description:
Patients will receive general anesthesia and the same intervention steps will be performed i.e., the block under investigation but instead of local anesthetic a placebo (2ml normal saline) will be injected (sham block)
Treatment:
Procedure: Sham group

Trial contacts and locations

1

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Central trial contact

Heba A. Mohamed, M.B.B.CH

Data sourced from clinicaltrials.gov

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