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study of the prophylactic effect of Dexamethasone on the headache after spinal anesthesia in patients undergoing cesarean

study of the prophylactic effect of Dexamethasone on the headache after spinal anesthesia in patients undergoing cesarean

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2013090314333N7
Enrollment
100
Registered
2013-10-12
Start date
2013-09-23
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Headache after spinal anesthesia. Spinal and epidural anaesthesia-induced headache during pregnancy

Interventions

Intervention 1: 0.15 mg Dexamethasone intravenous( per each kilogram of body weight) is prescribed to the intervention group immediately after cord clamping. Intervention 2: intravenous normal saline
Treatment - Drugs
0.15 mg Dexamethasone intravenous( per each kilogram of body weight) is prescribed to the intervention group immediately after cord clamping
intravenous normal saline is prescribed to the control group immediately after cord clamping

Sponsors

Vice Chancellor for Research Affairs, Kermanshah University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 35 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: patients aged 20 to 35; 150 to 170 cm in height; included in the ASA Class I and II and those signed a written consent. Exclusion criteria: All patients who were not included in ASA class I and II; patients didn’t sign the written consent; to have an underlying disease; complaining about any acute or chronic headache before spinal punctures; to use any analgesic drugs in the last two days; any contraindication to spinal anesthesia; to have a history of kidney, heart and lung diseases, or drug allergy.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Headache. Timepoint: 24 hours and seven days after surgery. Method of measurement: Asking the patients(mild,medium,high).

Countries

Iran (Islamic Republic of)

Outcome results

None listed

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