Actively Recruiting

Phase Not Applicable
Age: 18Years - 70Years
All Genders
NCT05282251

Intrapleural Nebulization of Bupivacain to Reduce Postoperative Pain

Led by Assiut University · Updated on 2024-05-20

60

Participants Needed

1

Research Sites

8 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Thoracic surgery is now common and as other surgeries evolution of minimally invasive techniques is employed. Video-assisted thoracic surgery (VATS) produces little scar but may produce severe pain that may affect the pulmonary function. Many procedure was developed like intercostal nerve block which require injections at multiple levels, Insertion of local anaesthetic (LA) in the surgical drain but that was dangerous due to the large amount of LA and not sufficient to completely eliminate pain. Bupvicaine nebulization, through surgical port which won't make any other wound, thought to be sufficient because Nebulization will enable us better distribution and less amounts of LA. Bupvicaine is local anaesthetic amide group that works by blocking sodium channels thus preventing progression of action potential.

CONDITIONS

Official Title

Intrapleural Nebulization of Bupivacain to Reduce Postoperative Pain

Who Can Participate

Age: 18Years - 70Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients classified as American Society of Anesthesiologists class 1 to 3
  • Scheduled for video-assisted thoracic surgery (VATS) under general anesthesia
Not Eligible

You will not qualify if you...

  • Allergy to local anesthetics
  • Pleural inflammation due to recent pneumonia
  • Unable or unwilling to perform spirometer test
  • Renal dysfunction with elevated creatinine greater than 2 mg/dl
  • Hepatic dysfunction with elevated liver enzymes three times above normal
  • History of addiction

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Assiut University

Asyut, Assuit, Egypt, 880

Actively Recruiting

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Research Team

E

Esam Moubarak Sahin

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

QUADRUPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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