Comparison of Fast track with routine regimen in reducting postoperative thoracotomy pain and respiratory complications
Early Phase 1
- Conditions
- Benign and Malignant disease of the lung, reduction of operative complications with regional anesthesia.J70, J94,
- Registration Number
- IRCT138902093831N1
- Lead Sponsor
- Tabriz University Of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 56
Inclusion Criteria
Both genders of patients with pulmonary disease which treated with elective thoracotomy, absence of blood coagulopathy, class I, II, or III American society of Anesthesiology, no underlying disease (pneumonia, Bronchitis, Asthma)
Exclusion criteria: class IV, V ASA, FE less than 40%, patients with Aortic stenosis, intraoperative bleeding more than 25% that needed blood transfusion, Time of Surgery more than three hours
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Post-thoracotomy pain. Timepoint: Daily until one week after surgery. Method of measurement: Respiratory postoperative pain and clinical symptom and signs (Pain seeing measurement).;ICU needed. Timepoint: Daily until one week after surgery. Method of measurement: Respiratory postoperative pain and clinical symptom.;Mechanical ventilation needed. Timepoint: Daily until one week after surgery. Method of measurement: Respiratory postoperative pain and clinical symptom.;Respiratory complications. Timepoint: Daily until one week after surgery. Method of measurement: Respiratory postoperative pain and clinical symptom.
- Secondary Outcome Measures
Name Time Method Mortality. Timepoint: Daily until one week. Method of measurement: Death rate.