Comparison of two drugs in the prevention ofheadache after spinal anaestesia
Phase 2
Recruiting
- Conditions
- Post dural puncture headache.Spinal and epidural anaesthesia-induced headache during labour and delivery
- Registration Number
- IRCT20120915010841N11
- Lead Sponsor
- Hamedan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 100
Inclusion Criteria
Patients aged 18 to 45 years old
candidates for cesarean section under spinal anesthesia
Physical ASA Class 1 and 2
Exclusion Criteria
Patients with a history of migraine headache
Sinusitis
Heart disease
Hypertension
Eclampsia and pre-eclampsia
Liver and kidney failure
History of corticosteroid use
Diabetes
Raynoode Phenomen
Spinal anesthesia contraindications (dissatisfaction, increased intracranial pressure, local infection, coagulopathy, anemia, hypovolemia, etc.)
Patients who do not have the necessary co-operation in answering questions
Those who are reluctant to continue to participate in the study
Patients who have failed spinal anesthesia and undergo general anesthesia
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Frequency of headache. Timepoint: During the surgery, the first 24 hours after surgery and one week after surgery. Method of measurement: Ask the patient.;Headache time. Timepoint: During the surgery, the first 24 hours after surgery and one week after surgery. Method of measurement: Ask the patient.;Headache severity. Timepoint: During the surgery, the first 24 hours after surgery and one week after surgery. Method of measurement: VAS of pain.;Duration of the headache. Timepoint: During the surgery, the first 24 hours after surgery and one week after surgery. Method of measurement: Ask the patient.
- Secondary Outcome Measures
Name Time Method