None listed
Conditions
Interventions
Intervention 1: Intervention group: receive 500 ml of 0.9% normal saline 30 minute before surgery. Intervention 2: Control group: do not receive fluid therapy before spinal anesthesia.
Prevention
Intervention group: receive 500 ml of 0.9% normal saline 30 minute before surgery.
Control group: do not receive fluid therapy before spinal anesthesia.
Sponsors
Vice chancellor for research,Neyshabur University of Medical Science
Eligibility
Sex/Gender
All
Age
20 Years to 85 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: No addiction; No history of migraine headache; Spinal anesthesia. Exclusion criteria: Patient dissatisfaction; Receiving different drugs or different doses of drug for spinal anesthesia.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Postdural Puncture Headache. Timepoint: 1 hour after intervention; 7 hour intervention; 24 hour after intervention; 7 days after intervention;. Method of measurement: Pain questionnaire. | — |
Secondary
| Measure | Time frame |
|---|---|
| Backache. Timepoint: 1 hour after intervention; 4 hour after intervention; 6 hour after intervention; 24 hour after intervention; 7 days after intervention. Method of measurement: Pain questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactSeyedeh Masoomeh Saadati
Neyshabur University of Medical Sciences
Outcome results
None listed