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Evaluation the efficacy of intravenouse propofol on post dural puncture headache incidence after cesarian section

Evaluation the efficacy of intravenouse propofol on post dural puncture headache incidence after cesarian section

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201603131616N5
Enrollment
120
Registered
2016-04-29
Start date
2014-03-21
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

Postdural Puncture Headache. Postdural Puncture Headache

Interventions

Intervention 1: Intervention group: After spinal anesthesia by left latral with Quincke spinal needle number 25 ,After leaving the infant propofol infuses with a pump at a rate of 30 micrograms per ki
Prevention
Treatment - Drugs
Intervention group: After spinal anesthesia by left latral with Quincke spinal needle number 25 ,After leaving the infant propofol infuses with a pump at a rate of 30 micrograms per kilogram per minut
In the control group no intervention was done The researcher must do completely control of BP, PR, RR, ECG,consciousness .

Sponsors

Vice chancellor for research, Kermanshah University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Exclusion criteria: history of headache. Housing consumption. opioid addiction . pulmonary/ heart disease. Diabetes. Other diseases that need treatment Inclusion criteria: pregnant women. Aged 18 -36. ASA class I, II.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Headache. Timepoint: 1,6,18,24 hours and 2,3,4,5,6,7 days after spinal anesthesia. Method of measurement: Visual Analogue Scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactRasoul Mahdavi Jafari

Kermanshah University of Medical Sciences

mahdjaf@gmail.com mahdjaf51@gmail.com+98 83 3427 6308

Outcome results

None listed

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