Spinal anesthesia additives
Phase 3
Recruiting
- Conditions
- additives in spinal anesthesia.Ovarian cyst, unilateral. unspecifiedN83.20
- Registration Number
- IRCT20230813059138N1
- Lead Sponsor
- niversity of Sousse, Faculty of Medicine Ibn Al Jazzar
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 120
Inclusion Criteria
Female
Age between (16-45 years)
ASA class 1 or 2
elective open unilateral ovarian cystectomy
Exclusion Criteria
spine deformity
bleeding tendency
neurological diseases
history of scorpion bite
patient disapproval
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Primary outcome were the onset and duration of both sensory and motor block, and the duration of spinal analgesia. Timepoint: 3 days after intervention. Method of measurement: sensory block by pinprick, while the motor block observed by modified bromage score.
- Secondary Outcome Measures
Name Time Method The secondary outcome were, nausea, vomiting, sedation, shivering, heart rate, mean arterial pressure. Timepoint: directly after intervention till 3 days after intervention. Method of measurement: inspection (visually) observation.