Lung Diseases Clinical Trial
— painOfficial title:
Comparison for Pethidine Requirement in Patients Received Spinal Morphine 0.2 and 0.3 Milligram for Post Lobectomy (Lung) Analgesia
Verified date | March 2012 |
Source | Mahidol University |
Contact | n/a |
Is FDA regulated | No |
Health authority | Thailand: Ethical Committee |
Study type | Interventional |
The purpose of the study is to evaluate the amount of total pethidine requirement during the 48 hour postoperative period after receiving spinal morphine 0.2 and 0.3 mg.
Status | Completed |
Enrollment | 40 |
Est. completion date | March 2012 |
Est. primary completion date | March 2012 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years to 70 Years |
Eligibility |
Inclusion Criteria: - Age > 18 year and < 70 year - Patient ASA physical status I-III. - Scheduled for thoracotomy with lobectomy. - Can operate a patient-controlled analgesia (PCA) device. Exclusion Criteria: - Known hypersensitivity to morphine or pethidine - History of bleeding tendency. - Known case of infection at the back - Patient refuse for spinal anesthesia - History of cerebrovascular disease. - Scheduled for video-assisted thoracoscopic lobectomy. - Need mechanical ventilatory support during postoperative period |
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Thailand | Faculty of Medicine, Siriraj Hospital | Bangkok |
Lead Sponsor | Collaborator |
---|---|
Mahidol University |
Thailand,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | pethidine requirement | Total pethidine requirement during 48 hours postoperative | 48 hours | Yes |
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