Comparing pain relief methods for thoracoscopic surgery
Comparison of Analgesic Effects of Ultrasound-guided Thoracic Paravertebral Block, Erector Spinae Muscle Block, Thoracic Paravertebral Block Combined with Erector Spinae Muscle Block, and Intercostal Nerve Block in Thoracoscopic Surgery
This study is testing different ways to manage pain after thoracoscopic surgery to see which method works best for patients.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 120 (estimated) |
| Ages | 18 Years to 70 Years |
| Sex | All |
| Sponsor | The First Hospital of Qinhuangdao Government |
| Locations | 1 site (Qinhuangdao, Hebei) |
| Trial ID | NCT06598852 on ClinicalTrials.gov |
What this trial studies
This study compares the effectiveness of various nerve block techniques for pain management in patients undergoing elective thoracoscopic surgery. A total of 120 patients will be randomly assigned to one of four groups: erector spinae muscle block, thoracic paravertebral block, a combination of both, or intercostal nerve block. Pain levels will be assessed using a visual analogue scale at multiple time points post-surgery, and various physiological parameters and adverse reactions will be monitored. The goal is to determine which method provides the best analgesic effect and minimizes postoperative complications.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18-70 with ASA Grade I-II who are scheduled for double-hole thoracic surgery.
Not a fit: Patients with severe heart disease, liver or renal insufficiency, or those with a history of chronic pain may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved pain management strategies for patients undergoing thoracoscopic surgery.
How similar studies have performed: Previous studies have shown varying success with similar nerve block techniques, indicating potential for effective pain management.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * (1) American Society of Anesthesiologists (ASA) Grade I-II; (2) Age: 18-70 years old (3) double-hole thoracic surgery was performed; (4) Agree to participate in this study and sign the informed consent. Exclusion Criteria: * (1) People who are allergic to anesthetics used in this study; (2) Patients with coagulation disorders (3) patients with severe heart disease, liver or renal insufficiency; (4) have a history of chronic pain or chronic opioid users (5) have a co-existing mental illness and are not fully capable of cooperating
Where this trial is running
Qinhuangdao, Hebei
- First hospital of Qinhuangdao — Qinhuangdao, Hebei, China (Recruiting)
Study contacts
- Study coordinator: Ximing Qi
- Email: qhdddyyykyc@163.com
- Phone: +86-13731777660
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.