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Solitary Mass clinical trials

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NCT ID: NCT01236495 Completed - Lung Diseases Clinical Trials

Comparison for Pethidine Requirement in Patients Received Spinal Morphine 0.2 and 0.3 mg for Post Lobectomy Analgesia

pain
Start date: November 2010
Phase: Phase 4
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.