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Clinical Trials/NCT05211791
NCT05211791RecruitingNot Applicable

Comparison Between Thoracic Epidural Anaesthesia, Erector Spinae Block and Paravertebral Block During Single-lung Ventilation for Lung Resection in Lateral Decubitus Position: A Prospective Randomized Study

South Egypt Cancer Institute2 sites in 1 country90 target enrollmentStarted: January 10, 2022Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Sponsor
Enrollment
90
Locations
2
Primary Endpoint
peri-operative analgesia

Study Overview

Brief Summary

Thoracotomy operations are known to be painful surgical procedures, so providing effective intraoperative and postoperative analgesia is so important for all anaesthesiologists. Ineffective pain management interferes with deep breathing, coughing, and remobilization resulting in atelectasis and pneumonia.

Ultrasound-guided ESP block is a myofascial plane block that provides analgesia for thoracic or abdominal segmental innervation depending on the level of the injection site. Thoracic epidural analgesia (TEA) is considered the gold standard analgesic technique for thoracic surgeries. But the invasiveness of this technique, the rare but serious neurologic complications and the failure rates up to 30% are the disadvantages of epidural analgesia

Detailed Description

The aim of this study is to compare the effect of different blocks as TEA, erector spinae block or paravertebral block on improving peri-operative analgesia and post-operative outcome in pulmonary resection in adult patients.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
Triple (Participant, Care Provider, Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to 70 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • aged between 18 to 70 years old for elective lung resection. with American Society of Anesthesiology physical status (ASA-PS) I-III

Exclusion Criteria

  • Total pneumonectomy
  • Hepatic or renal dysfunction.
  • contraindications for epidural anesthesia as Coagulopathy and neurological and spinal deficits.
  • emergency cases

Outcomes

Primary Outcomes

peri-operative analgesia

Time Frame: up to 48 hours postoperative

Visual Analogue score (resting and during cough) from 0 (no pain) to 10 (worst pain pain measurement

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
South Egypt Cancer Institute
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Alaa Ali M. Elzohry

Lecturer of Anesthesia, ICU and Pain Relief, South Egypt Cancer Institute, Assiut University, Egypt

South Egypt Cancer Institute

Study Sites (2)

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