Cesarean section. Complications of anaesthesia during labour and delivery
Conditions
Interventions
Intervention 1: Intervention group: Patients were randomly allocated to receive intrathecally either 10mg Hyperbaric Bupivacaine plus 0.1ml(50mg) sulfate magnesium 50%. Intervention 2: Control group:P
Treatment - Drugs
Intervention group: Patients were randomly allocated to receive intrathecally either 10mg Hyperbaric Bupivacaine plus 0.1ml(50mg) sulfate magnesium 50%
Control group:Patients with 10 mg Intrathecal Bupivacaine with 0.1 ml of normal saline is injected.
Sponsors
Vice-chancellor Of Research Babol University Of Medical Sciences
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: Inclusion criteria: ASA class I,II; Height 160 to 180 cm; candidates for elective caesarean section; gestational age over 39 weeks Exclusion criteria: Patients with a history of cardiovascular disease; psychiatric; chronic pain; dependent on drugs and alcohol; HTN; DM and other systemic disease.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Evaluation of Sensory block duration. Timepoint: Sensory block level evaluated every 30 second until 15 minutes and then 5 minutes until sensory block off. Method of measurement: Needle No 20.;Evaluation of motor block duration. Timepoint: motor block level evaluated every 30 second until 15 minutes and then 5 minutes until motor block off. Method of measurement: Bromage scale. | — |
Secondary
| Measure | Time frame |
|---|---|
| Blood pressure. Timepoint: 0, 1, 3, 6, 9, 12, 15, 18 and 21 min. Method of measurement: Non Invasive BP.;Heart rate. Timepoint: 0, 1, 3, 6, 9, 12, 15, 18 and 21 min. Method of measurement: ECG.;Analgesia. Timepoint: first 24 hours after spinal. Method of measurement: VAS. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactDr Bahman Hasannasab
Babol University Of Medical Sciences
Outcome results
None listed