Actively Recruiting
TPVB or SPSIPB in Pain Management After VATS
Led by Koç University · Updated on 2025-01-03
44
Participants Needed
1
Research Sites
10 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The goal of this clinical trial is to compare the analgesic efficacy of thoracal paravertebral block (TPVB) and serratus posterior superior intercostal plane block (SPSIPB) in patients undergoing video-assisted thoracoscopic surgery (VATS). The main questions it aims to answer are: How will the total perioperative opioid consumption of the patients receiving two different blocks change? How will TPVB and SPSIPB effect the patients' numeric rating scores for pain in the postoperative 24-hour period? How will TPVB and SPSIPB effect the incidence of opioid related side effects? Participants will be divided in two groups: TPVB group will receive a TPVB before the surgery. SPSIPB group will receive a SPSIPB nerve block before the surgery. Researchers will compare the results between the groups to see the postoperative effects concerning opioid consumption as well as the pain scores, respiratory parameters and opioid associated side effects. The hypothesis of this study is that participants receiving SPSIPB for VATS will have a less total opioid consumption 24 hours postoperatively.
CONDITIONS
Official Title
TPVB or SPSIPB in Pain Management After VATS
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients between the age of 18-80 undergoing video-assisted thoracoscopic surgery
You will not qualify if you...
- Allergy to local anaesthetics
- Chronic opioid use history
- Patients with psychiatric disorders
- Patients who are not open to communication
- Patients with chronic organ failure
- Patients that do not give consent
- Patients that need emergency surgery within the first 24 hours of the initial surgery
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Koc University
Istanbul, Turkey (Türkiye), 34010
Actively Recruiting
Research Team
K
Kamil Darçın, MD
CONTACT
Y
Yasemin Sincer, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
OTHER
Number of Arms
2
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here