The Effect Of Multimodal Analgesia On Chronic Pain
CompletedNCT02660749
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)
This study aimed to show the characteristics and predictors of chronic pain after a mini-thoracotomy. Non-Coronary Heart Surgery patients were scheduled for the study. In patients with acute postoperative period use of tramadol retard, metamizole, and dexketoprofen the effects on the development of chronic pain and its character have been analyzed.
Study details
- Official title
- The Effect Of Tramadol, Metamizol and Dexketoprofen Combination On Chronic Pain Development After Heart Surgery
- Conditions
- Heart Surgery
- Sponsor
- Tobb University of Economics and Technology
- Start date
- 2015-05
- Primary completion
- 2016-09
- Sex
- All
- Age range
- from 20 Years to 70 Years
- Healthy volunteers
- true
- Results posted
- No results posted in this snapshot
- Total sites listed
- 0
Eligibility criteria
Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * Patients included between 20-70 years * ASA 1-4 * Euroscore value lower than 7 * Undergoned non coronary heart surgery (minithoracotomy) * Intensive care has been discharged from the service in 24 hours , with patients given tramadol retard , metamizol, Dexketoprofen on postoperatif first day to discharged from the hospital. Exclusion Criteria: * Diabetes mellitus * Chronic renal failure * COPD * Uncontrolled hypertension * Epilepsy * Psychiatric disease * Malignancy * Patients with a history of cerebrovascular disease * Patients with ischemia * Patients suffering from chronic pain and analgesic use * Patients taking antidepressants and antiepileptic drug * Off-pump technique used or redo undergo cases * Ongoing postoperative time thoracic or mediastinal drains more than 48 hours remaining patients, bleeding or patients who received repeated revisions due to infection * More than 24 hours remaining in intensive care patients * Patients with long discharge duration 1 week * Patients who discontinued due to side effects of tramadol may begin after medicines. * Postoperative wound infection.
Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT02660749