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Effect of intravenous aminophylline on post- spinal anesthesia headache in women under cesarean section

Effect of intravenous aminophylline on post- spinal anesthesia headache in women under cesarean section

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180607040003N1
Enrollment
70
Registered
2018-09-03
Start date
2018-04-21
Completion date
Unknown
Last updated
2018-10-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Headache. Other headache syndromes

Interventions

Intervention 1: Intervention group: Headache before giving aminophylline in the aminofilin dose group. In this study, 3 cc per kg body weight of the drug are given at the diagnosis of the headache, an

Sponsors

Gonabad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: Satisfaction to participate in the study Subjected to cesarean section with spinal anesthesia No history of sensitivity to aminophylline or other xanthine derivatives with accurate history from them. Age 45-18 years Lack of history of migraine headaches, coagulation disorders, gestational toxicity, diabetes, seizure, smoking and narcotics, and cardiovascular diseases

Exclusion criteria

Exclusion criteria: Performing a retinal anxiety Unwillingness to cooperate in the study General anesthesia Use of xanthine derivatives during the study

Design outcomes

Primary

MeasureTime frame
Headache. Timepoint: 24h. Method of measurement: observation.

Countries

Iran (Islamic Republic of)

Contacts

Public Contacthoseyn bayeste

Gonabad University of Medical Sciences

m.eshaghzadeh93@gmail.com+98 51 5222 6013

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026