Trials / Completed
CompletedNCT01236495
Comparison for Pethidine Requirement in Patients Received Spinal Morphine 0.2 and 0.3 mg for Post Lobectomy Analgesia
Comparison for Pethidine Requirement in Patients Received Spinal Morphine 0.2 and 0.3 Milligram for Post Lobectomy (Lung) Analgesia
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 40 (actual)
- Sponsor
- Mahidol University · Academic / Other
- Sex
- All
- Age
- 18 Years – 70 Years
- Healthy volunteers
- Not accepted
Summary
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.
Detailed description
Thoracotomy causes severe pain to the patients. Continuous thoracic epidural is a gold standard for postoperative pain. However, it needs skill. There are many alternatives such as spinal morphine, intercostal nerve block, cryoalangesia or interpleural block.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | spinal morphine 0.3 mg | spinal morphine 0.3 mg |
| DRUG | spinal morphine 0.2 mg | spinal morphine 0.2 mg |
Timeline
- Start date
- 2010-11-01
- Primary completion
- 2012-03-01
- Completion
- 2012-03-01
- First posted
- 2010-11-08
- Last updated
- 2012-03-13
Locations
1 site across 1 country: Thailand
Source: ClinicalTrials.gov record NCT01236495. Inclusion in this directory is not an endorsement.