Comparing pain relief methods after mastectomy surgery
Comparison of the Postoperative Analgesic Effects of Serratus Posterior Superior Intercostal Plane Block and Thoracic Paravertebral Block in Mastectomy Operations
This study tests two different pain relief methods after mastectomy surgery to see which one helps patients feel better and need less opioid medication.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 60 (estimated) |
| Ages | 18 Years to 80 Years |
| Sex | Female |
| Sponsor | Ankara Etlik City Hospital Government |
| Locations | 1 site (Yenimahalle, Ankara) |
| Trial ID | NCT06789146 on ClinicalTrials.gov |
What this trial studies
This study aims to evaluate the effectiveness of two different nerve block techniques, the serratus posterior superior intercostal plane block and the thoracic paravertebral block, in managing postoperative pain for patients undergoing mastectomy. By comparing these methods, the study seeks to determine which technique provides better analgesic effects and reduces the need for opioid medications. The goal is to enhance patient recovery and quality of life following breast cancer surgery.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 18-80 with an ASA score of I-III and a BMI between 18-30 kg/m2.
Not a fit: Patients outside the age range of 18-80, those with an ASA score of IV or higher, or those with a BMI below 18 or above 30 kg/m2 may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved pain management strategies for mastectomy patients, reducing reliance on opioids and enhancing recovery.
How similar studies have performed: Previous studies have shown promising results with similar nerve block techniques in managing postoperative pain, indicating that this approach is supported by existing evidence.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients aged 18-80 years * American Society of Anesthesiologists (ASA) score I-II-III * Body Mass Index (BMI) between 18-30 kg/m2 Exclusion Criteria: * Patients under 18 and over 80 years of age * ASA score IV and above * Patients with a history of bleeding diathesis * BMI below 18 or above 30 kg/m2
Where this trial is running
Yenimahalle, Ankara
- Ankara Etlik City Hospital — Yenimahalle, Ankara, Turkey (Recruiting)
Study contacts
- Study coordinator: Atakan Sezgi, MD
- Email: kansezgi@gmail.com
- Phone: 00905323327000
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.