Actively Recruiting
ITPB 1 vs 3 in VATS
Led by Chinese University of Hong Kong · Updated on 2025-04-11
80
Participants Needed
1
Research Sites
60 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This study aims to evaluate the quality of recovery after video-assisted thoracoscopic surgery (VATS) by comparing the efficacy of a single-level intertransverse process block (ITPB) against a three-level ITPB, with particular attention to the quality of recovery measured by the QoR15 score at 24 hours post-surgery.
CONDITIONS
Official Title
ITPB 1 vs 3 in VATS
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients aged 18 to 80 years
- ASA physical status classification I to III
- Patients with primary lung carcinoma scheduled for resection using VATS procedure
You will not qualify if you...
- Patient refusal to participate
- Local skin infection at the planned injection site
- Known coagulopathy or bleeding disorder
- History of allergy to local anesthetics
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Department of Anaesthesia, Pain and Perioperative Medicine, Prince of Wales Hospital, Shatin
New Territories, Hong Kong
Actively Recruiting
Research Team
A
Ayla Wong, RN, BN
CONTACT
M
Manoj K Karmakar, MD, FRCA
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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