Actively Recruiting

Phase Not Applicable
Age: 18Years - 70Years
All Genders
Healthy Volunteers
NCT06856538

Rhomboid Intercostal Sub Serratus Plane Block Versus Serratus Anterior Plane Block in Thoractomy

Led by Yasser S Mostafa, MD · Updated on 2025-03-06

40

Participants Needed

1

Research Sites

86 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The objective of the current study is to compare the efficacy of the analgesic effect of ultrasound-guided unilateral Rhomboid intercostal and sub serratus plane block (RISS) versus Serratus anterior plane block (SAPB) in Thoracotomy incision.

CONDITIONS

Official Title

Rhomboid Intercostal Sub Serratus Plane Block Versus Serratus Anterior Plane Block in Thoractomy

Who Can Participate

Age: 18Years - 70Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients aged 18-70 years
  • Scheduled for unilateral thoracotomy
  • American Society of Anesthesiologists (ASA) physical status I-III
  • Candidates for general anesthesia
  • No history of severe allergies to local anesthetics or other medications used during the procedure
Not Eligible

You will not qualify if you...

  • ASA physical status class IV or higher
  • Obesity with BMI 35 or greater
  • Uncontrolled cardiovascular conditions
  • Neurological deficits, cardiopulmonary, hepatorenal, or metabolic diseases
  • Use of anticoagulants or presence of any drug allergies
  • Emergency or repeat surgeries
  • Systemic infections or infections at the injection site
  • Psychiatric illnesses including schizophrenia, bipolar disorder, uncontrolled anxiety or depression
  • Narcotic dependency

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

Fayoum University hospital

El Fayoum Qesm, Faiyum Governorate, Egypt, 63514

Actively Recruiting

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Research Team

E

Emad El Mohamed Abd El-Razek, M.Sc.

CONTACT

Y

Yasser S Mostafa, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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