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Spinal anesthesia in patients with cesarean section

A Comparative Study on the Effect of Combined Fentanyl and Midazolam with Propofol Infusion on Blood Pressure and Heart Rate and Satisfaction of Cesarean Patients under Spinal Anesthesia

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT201701277745N6
Enrollment
150
Registered
2017-07-07
Start date
2016-11-30
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

Spinal Anesthesia in pregnant patient. 094-099

Interventions

Spinal anesthesia: Lidocaine 5% at a dose of 75 mg at the start of C/S plus 50 micro-gram Fentanyl Propofol: was infused at a rate of 8 mg per Kg/h Fentanyl was infused at a rate of 0.5 micrograms
Prevention
Spinal anesthesia: Lidocaine 5% at a dose of 75 mg at the start of C/S plus 50 micro-gram Fentanyl Propofol: was infused at a rate of 8 mg per Kg/h Fentanyl was infused at a rate of 0.5 microgram

Sponsors

Deputy of Research and Technology
Lead Sponsor
Deputy of Research and Technology
Collaborator

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Inclusion: Pregnant mothers who come to the operating room for non-emergency surgery to undergo surgery. Exclusion: Patients with a history of diabetes, addiction, high blood pressure or antihypertensive drug use, and also at the time of surgery for maintaining hemodynamic status using drugs that increase blood pressure and heart rate

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Heart rate and blood pressure. Timepoint: The patient's arrival time to the operating room, before the spinal anesthesia, every 10 minutes of badness for spinal anesthesia up to 60 minutes. Method of measurement: Using a blood pressure monitor and heart rate monitor.

Secondary

MeasureTime frame
Satisfaction and a pleasant feeling by the mother. Timepoint: After the surgery and recovery time. Method of measurement: The question of patient.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAfshin Mansourian

YUMS

afshin.mansourian@yahoo.com+98 74 3322 0166

Outcome results

None listed

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