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Taking people in EgyptNo phase

Two Nerve Block Methods for Pain Relief During Lung Cancer Surgery

Compares two nerve block techniques in adults having chest surgery for lung cancer.

Plain-language title generated from the registry record
Registry title: Costotransverse Foramen Block Versus Thoracic Paravertebral Block in Thoracotomy for Lung Cancer

Key facts

Where
Cairo, EgyptSee the site

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 65 years old?

Source: NCT07367581, who can take part

Where in Egypt

  • Cairo UniversityCairo, EgyptTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
National Cancer Institute, Egypt
Trial code
NCT07367581
Record updated
27 January 2026
Original description
This study aims to compare the costotransverse foramen block (CTFB) with thoracic paravertebral block (TPVB) in patients undergoing thoracotomy for lung cancer.Read full original descriptionShow less

Costotransverse Foramen Block Versus Thoracic Paravertebral Block in Thoracotomy for Lung Cancer: A Randomized Controlled Trial

This study aims to compare the costotransverse foramen block (CTFB) with thoracic paravertebral block (TPVB) in patients undergoing thoracotomy for lung cancer.

Inclusion: Age > 18 years and ≤ 65 years old; American Society of Anesthesiologists (ASA) physical status II-III; Body mass index 18-35 kg/m2; Patients scheduled for thoracotomies for lung cancer.

Exclusion: Patients on chronic pain therapy; History of sensitivity to local anesthetics; History of psychological disorders; Severe respiratory, cardiac, hepatic, or renal disease; Patient refusal; Contraindication to regional anesthesia, e.g., local sepsis, pre-existing peripheral neuropathies, and coagulopathy; Morbid obesity; Uncooperative patients.

ClinicalTrials.gov NCT07367581