Clinical Trials Directory

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

TypeNameDescription
DRUGspinal morphine 0.3 mgspinal morphine 0.3 mg
DRUGspinal morphine 0.2 mgspinal 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.