Understanding chronic pain after sternotomy surgery
Incidence of Chronic Pain After Sternotomy
This study looks at how many people experience long-lasting pain after heart surgery and what might cause it, focusing on patients aged 18 to 80.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 200 (estimated) |
| Ages | 18 Years to 80 Years |
| Sex | All |
| Sponsor | Ankara City Hospital Bilkent Academic / other |
| Locations | 1 site (Çankaya, Ankara) |
| Trial ID | NCT05357963 on ClinicalTrials.gov |
What this trial studies
This observational study aims to investigate the incidence and risk factors associated with chronic pain following sternotomy operations. It focuses on patients aged 18 to 80 who are undergoing elective sternotomy, assessing their pain levels three months post-surgery. The study seeks to fill the gap in epidemiological data regarding chronic postoperative pain, which can significantly impact patients' quality of life. By analyzing these findings, the research hopes to provide insights into the prevalence of chronic pain in this patient population.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 18 to 80 who are scheduled for elective sternotomy and have a physical status classified as I to IV by the American Society of Anesthesiologists.
Not a fit: Patients with a history of chronic analgesic therapy, previous sternotomy surgeries, or those undergoing emergency operations may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved management strategies for chronic pain in patients after sternotomy, enhancing their quality of life.
How similar studies have performed: While chronic postoperative pain is a recognized issue, this study addresses a specific gap in the literature regarding sternotomy, making it a novel investigation.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Age between 18 and 80 years * American Society of Anesthesiologists' physical status I-II-III-IV * Body mass index (BMI) between 18-35 kg/m2 * Patients undergoing elective sternotomy Exclusion Criteria: * History of chronic analgesic therapy * Patients with previous sternotomy surgery * Patients who were operated under emergency conditions
Where this trial is running
Çankaya, Ankara
- Ankara City Hospital — Çankaya, Ankara, Turkey (Recruiting)
Study contacts
- Principal investigator: Nilgün ZENGİN, MD — Ankara City Hospital Bilkent
- Study coordinator: Nilgün ZENGİN, MD
- Email: nilbavullu@gmail.com
- Phone: +905063370548
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.