Complications predominantly related to the anesthesia. Other complications of spinal and epidural anaesthesia
Conditions
Interventions
Intervention 1: Intervention 1: First group receive placebo Supp. and 2cc of IV hydrocortison, 10 min before anesthesia. Intervention 2: Intervention 2: Second group receive 100mg Diclofenac supp and
Prevention
Intervention 1: First group receive placebo Supp. and 2cc of IV hydrocortison, 10 min before anesthesia.
Intervention 2: Second group receive 100mg Diclofenac supp and 2cc of normal saline, 10 min before anesthesia .
Intervention 3: Third group receive placebo Supp and 2cc of IV normal saline, 10 min before anesthesia .
Sponsors
Vice Chancellor for Research of Qazvin University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
17 Years to 40 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: pregnant women who candidate for elective cesarean section; ASA class 1, 2. Exclusion criteria: history of asthma; peptic ulcer; febrile disease, or endocrine disease; addiction to opioid; smoking; consumption of steroids; consumption of NSAIDS or other analgesics.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Shivering. Timepoint: 10 min before anesthesia, after surgery and every 30 minute until an hour. Method of measurement: observation and medical records. | — |
Secondary
| Measure | Time frame |
|---|---|
| Temperature. Timepoint: 10 min before anesthesia, after surgery and every 30 minute until one hour. Method of measurement: Thermometery from tympanic membrane.;Blood pressure. Timepoint: 10 min before anesthesia, after surgery and every 30 minute until one hour. Method of measurement: With manonetery from brachial artery.;Pulse rate. Timepoint: 10 min before anesthesia, after surgery and every 30 minute until one hour. Method of measurement: With monitoring. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactDr. Marziyeh Beigom Khezri
Kowsar Hospital
Outcome results
None listed