Compare the effect of preloading in spinal anesthesia
Not Applicable
- Conditions
- The effect of pretreatment with various solutions at the level of sensory block in the spinal anesthesia.-
- Registration Number
- IRCT2015121616956N7
- Lead Sponsor
- Vice chancellor for research,tabriz University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
all patients 20 to 70 years, scheduled for lower abdominal surgery with spinal anesthesia: ASA I-II
Excinclusion criteria: the inability to collaborate and determine the level of anesthesia by patients: patients with Spinal disorder and deformity: contraindications to spinal anesthesia: contraindications for use of voluven: lack of consent and cooperation of the patient: patients needing transfusion or infusion of additional fluids during surgery due to hemodynamic instability
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Sensory block level. Timepoint: Every 5 minutes to 30 minutes and then 60 minutes after spinal anesthesia and 90. Method of measurement: pinprick test.
- Secondary Outcome Measures
Name Time Method Headache. Timepoint: Postoperative. Method of measurement: Ask the patient.;Blood pressure. Timepoint: Every 5 minutes to 30 minutes and then every 15 minutes until the end of surgery. Method of measurement: By monitoring.;Heart rate. Timepoint: Every 5 minutes to 30 minutes and then every 15 minutes until the end of surgery. Method of measurement: By monitoring.