Chronic Post Surgical Pain-Cardiac
CompletedNCT06382077
View the official record on ClinicalTrials.gov Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.
This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.
Brief summary (from the registry)
The CPSP-Cardiac is a large, multi-center, observational study with the aim to investigate the incidence of chronic pain in the 3rd month postoperatively in cardiac surgery and its affecting factors.
Study details
- Official title
- Determination of the Frequency and Affecting Factors of Chronic Postsurgical Pain After Cardiac Surgery: A Multicenter, Observational Study
- Conditions
- Sponsor
- Ondokuz Mayıs University
- Start date
- 2024-05-07
- Primary completion
- 2025-08-01
- Sex
- All
- Age range
- from 18 Years to 80 Years
- Results posted
- No results posted in this snapshot
- Countries
- Turkey (Türkiye)
- Total sites listed
- 29
Eligibility criteria
Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * patients will be undergoing a first-time cardiac surgery involving a median sternotomy, including coronary artery bypass grafting (CABG) and all open-heart procedures, such as valvular repairs/replacement. * patients between the ages of 18-80 years * American Society of Anesthesiologists (ASA) Physical Status score of II-III * patients will also sign the written informed consent form Exclusion Criteria: * patients scheduled for minimally invasive cardiac surgery, * patients with BMI\>40, * patients who undergone thoracotomy, * patients with alcohol and drug addiction, * patients with severe dysfunction in a significant organ (e.g., presence of severe hepatic and renal disease), * patients who undergone emergency and redo surgeries, * patients who cannot be extubated within the first 8 hours postoperatively, * patients have a severe psychiatric diseases such as psychosis or dementia that restrict cooperation with the patient (patients who cannot evaluate verbal numerical pain scales), * patients who are pregnant and breastfeeding, * patients who cannot be reached by phone during the postoperative follow-up periods * patients who cannot communicate in the native language.
Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT06382077