Comparing pain management techniques during video-assisted thoracic surgery
QORVATS Study. A Randomized Controlled, Triple Blinded to Compare the Quality of Recovery (QoR 40) Between Intercostal Block and a Combination of Intercostal Nerve Block With Serratus Plane Catheter for Patient's Undergoing VATS Procedures.
NA · London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's · NCT04990713
This study is testing whether a local anesthetic can help reduce pain and improve recovery for patients having video-assisted thoracic surgery compared to a placebo.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 200 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's (other) |
| Locations | 1 site (London, Ontairo) |
| Trial ID | NCT04990713 on ClinicalTrials.gov |
What this trial studies
This clinical trial evaluates the effectiveness of two pain management techniques for patients undergoing video-assisted thoracic surgery (VATS). Participants will be randomly assigned to receive either a local anesthetic or a placebo in addition to standard care. The study aims to assess postoperative pain levels and the impact on recovery outcomes. It employs a triple-blind methodology to ensure unbiased results, with blinding for participants, clinical teams, and data collectors.
Who should consider this trial
Good fit: Ideal candidates include adults over 18 years old undergoing elective VATS lung resections with an ASA score of 1 to 4.
Not a fit: Patients who may not benefit include those with allergies to local anesthetics, emergency surgery needs, or chronic pain conditions.
Why it matters
Potential benefit: If successful, this study could lead to improved pain management strategies, enhancing recovery and reducing hospital readmissions for patients undergoing VATS.
How similar studies have performed: Previous studies have shown varying success with similar analgesic techniques, but this specific comparison is novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients undergoing elective VATS lung resections including wedge resection, segmentectomy, bi-lobectomy, or lobectomy. * Age \> 18 years. * ASA (American Society of Anesthesiology) Score - 1 to 4. * Gender - all genders * Patients able to consent to participate in the study Exclusion Criteria: * Patient refusal to participate in the study. * Emergency surgery. * Allergies to local anesthetics * BMI\>40 * Presence of local (chest wall) or systemic infection. * Previous lung resection on the same hemithorax. * Patient suffering from chronic pain defined by persistent pain more than six month. * Conversion to thoracotomy
Where this trial is running
London, Ontairo
- London Health Sciences Centre — London, Ontairo, Canada (RECRUITING)
Study contacts
- Principal investigator: Abhijit Biswas, MD — Western University, Canada
- Study coordinator: Abhijit Biswas, MD
- Email: abhijit.biswas@lhsc.on.ca
- Phone: 5196858500
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Video Assisted Thoracic Surgery, Pain Management, Intercostal Block, Fascial Plane Block