Clinical study of treatment for intercostal neuralgia developed after thoracotomy
Phase 2
- Conditions
- thoracotomy
- Registration Number
- JPRN-UMIN000006672
- Lead Sponsor
- Teikyo University, School of Medicine, Department of Surgery
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 68
Inclusion Criteria
Not provided
Exclusion Criteria
(1) patients who have been taking antidepressants, anticonvulsant, opoids, and NSAIDs before surgery (2) patients who have serious complications (such as uncontrollable heart, lung, liver or kidney disease, and diabetes) (3) patients who have a history of angioedema (4) patients who are pregnant, are nursing, or might be pregnant (voluntary) (5) patients who handle hazardous machinery, such as driving a car (6) patients who are considered unsuitable for the study by the primary physician
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method -Control rate of pain at the incision site after surgery; NRS on the third month after surgery
- Secondary Outcome Measures
Name Time Method -Control rate of pain at the incision site after surgery; NRS on the first, third, and seventh day after surgery, VAS in the fourth and eighth week after surgery -Control the level of pain according to the type of pain (neurophathic pain or nociceptive pain) - Occurrence rate of adverse event