Status:
COMPLETED
Discharge Conditions of Spinal Anesthesia With Heavy Prilocaine-Fentanyl and Heavy Bupivacaine-Fentanyl
Lead Sponsor:
Diskapi Teaching and Research Hospital
Conditions:
Hemorrhoid
Peri Anal Fistula
Eligibility:
All Genders
18-70 years
Phase:
PHASE4
Brief Summary
In this prospective randomized study the investigators aimed to investigate difference of the duration of spinal anesthesia, discharge times and efficacy between low dose heavy Prilocaine-Fentanyl and...
Detailed Description
ASA status I-III patients will be recruited. Patients will be randomized in two groups. Group B will be received 1.5 ml heavy bupivacaine+ 20 mic fentanyl+ 0.15 ml and Group P will be received 1,5 ml ...
Eligibility Criteria
Inclusion
- ASA status I-III
Exclusion
- Patients with contraindications for spinal anesthesia,
- hypersensitivity to study drugs
Key Trial Info
Start Date :
April 1 2012
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
July 1 2013
Estimated Enrollment :
50 Patients enrolled
Trial Details
Trial ID
NCT01880775
Start Date
April 1 2012
End Date
July 1 2013
Last Update
June 3 2014
Active Locations (1)
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1
Diskapi Yildirim Beyazit Training and Research Hospital
Ankara, Turkey (Türkiye), 06110