Comparing two pain relief methods after chest surgery
Effects of Erector Spina Plane Block and Paravertebral Block on Early Postoperative Pulmonary Function Test Parameters in Patients Undergoing Video-assisted Thoracoscopic Surgery
This study is testing two different pain relief methods after chest surgery to see which one helps patients recover better and breathe easier.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 70 (estimated) |
| Ages | 18 Years to 65 Years |
| Sex | All |
| Sponsor | Başakşehir Çam & Sakura City Hospital Government |
| Locations | 1 site (Istanbul) |
| Trial ID | NCT06584201 on ClinicalTrials.gov |
What this trial studies
This study evaluates the effectiveness of two pain management techniques, Erector Spinae Plane Block (ESP) and Paravertebral Block (PVB), in patients undergoing Video-assisted Thoracoscopic Surgery (VATS). The focus is on how these methods impact lung function and postoperative recovery. By measuring changes in respiratory function before and after surgery, the study aims to identify which analgesic technique leads to better outcomes in terms of pain control and lung health. The goal is to enhance recovery and minimize complications associated with pain after surgery.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18 to 65 with ASA physical status I-III who are undergoing minimally invasive chest surgery.
Not a fit: Patients with severe comorbidities, chronic pain conditions, or those unable to cooperate with postoperative follow-ups may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved pain management strategies that enhance lung function and accelerate recovery for patients after chest surgery.
How similar studies have performed: Previous studies have shown promising results with similar analgesic techniques, suggesting potential for success in this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Both genders * Being between the ages of 18 and 65 * ASA(American Society of Anesthesiologists) I-II-III * Body mass index between 19 and 30kg/m2 * Providing voluntary participation * Must be fully oriented and able to cooperate Exclusion Criteria: * ASA(American Society of Anesthesiologists) IV-V * Patients who refuse to participate in the study * Patients under 18 years of age * Patients over 65 years of age * Presence of active infection in the area to be treated * Chronic pain and constant analgesic use * Patients with coagulation disorders * Patients who cannot cooperate with postoperative pain follow-ups * Cases taken urgently * Patients with severe renal failure (creatinine\>2mg/dl) * Severe impairment of heart function (New York Heart Association Functional Classification III-IV) * Patients with known allergies to bupivacaine and other amide local anesthetic substances.
Where this trial is running
Istanbul
- Basaksehir Çam Ve Sakura City Hospital — Istanbul, Turkey (Türkiye) (Recruiting)
Study contacts
- Study coordinator: Özal Adiyeke
- Email: ozaladiyeke@gmail.com
- Phone: 00905377398652
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.