The Effect Of Spinal Anesthesia Drug to Prevent Maternal Hypotentio
Not Applicable
- Conditions
- Maternal hypotension.maternal hypotension syndrome
- Registration Number
- IRCT201704183305N8
- Lead Sponsor
- Vice chancellor research for Babol University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 105
Inclusion Criteria
pregnant women, candidate for elective CS, in class I physical health classification of the American Society of Anesthesia (ASA). All women had singleton term pregnancies.
Exclusion criteria: Mothers with a history of hypertension, diabetes, cardiovascular and cerebral diseases, known fetal anomaly, any kind of contraindications for spinal anesthesia, patients weighing over 100 kg and those with dificult tracheal intubation.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Maternal blood presure. Timepoint: Maternal blood pressure was monitored and recorded every two minutes for the first 15 minutes following spinal anesthesia, and then every 5 minutes until completion of surgery. Method of measurement: Non invasive blood presure cuff.
- Secondary Outcome Measures
Name Time Method Sensory level and motor block. Timepoint: After spinal anesthesia. Method of measurement: Sensory level was assessed using the tip of a needle sterilized with alcohol cotton, and motor block was assessed and recorded using Bromage Scale (BS) (BS=0, full knee and foot flexion; BS=1, ability to move knee; BS=2, ability to move feet only; BS=3, full motor block).;Pain. Timepoint: Pain level during surgery. Method of measurement: VAS (Visual analogues Scale).;Return of sensory and motor block. Timepoint: After Surgery. Method of measurement: Examination, Question & Observation.