The Optimal Effect Site Concentration of Propofol for Conscious Sedation in Elderly Male Patients Undergoing Urologic Surgery Under Spinal Anesthesia With or Without Intrathecal Fentanyl
Clinical trial NCT01232270 · COMPLETED
Trial details
- NCT number
- NCT01232270
- Sponsor
- Yonsei University
- Status
- COMPLETED
- Phase
- Not Applicable
- Study type
- INTERVENTIONAL
- Start date
- 2010-10-01
- Primary completion
- 2011-07-01
- Enrollment
- 43
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