Spinal anesthesia. Spinal and epidural anaesthesia-induced headache during pregnancy
Conditions
Interventions
Intervention 1: Control Group: anesthesia was in sitting position and location of the L3-L4, L4-L5 with a disposable 25-gauge needle with 75 mg lidocaine 5% and 25 mcg of fentanyl. Intervention 2: Int
Treatment - Drugs
Control Group: anesthesia was in sitting position and location of the L3-L4, L4-L5 with a disposable 25-gauge needle with 75 mg lidocaine 5% and 25 mcg of fentanyl.
Intervention group: intraoperative injection of intravenous dexamethasone 8mg
Sponsors
Vice Chancellor for Research, Gonabad University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
20 Years to 40 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: To be ready to join in trial; age between 20 - 40 years; cesarean section under spinal anesthesia; physical status be class I and EI according to ASA; no history of psychological disease; no history of migraine or backache. Exclusion criteria: Another anesthesia or any other surgery during the week of study.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Headache. Timepoint: First 24 hours and first week. Method of measurement: Questionnaire.;Backache. Timepoint: First 24 hours and first week. Method of measurement: Questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactDr. Arash Hamzei
Gonabad University of Medical Sciences
Outcome results
None listed