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The effect of anesthesia on apgar score and maternal hemodynamic parameters after cesarean

The comparsion of propofol , thiopental with thiopental- propofol as induction drug on hemodynamic parameters of parturients and neonatal apgar during elective cesarean section

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201503166808N6
Enrollment
84
Registered
2015-11-19
Start date
2015-02-09
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

caesarean. Delivery by elective caesarean section

Interventions

Intervention 1: In propofol group, propofol 2 mg /kg Intravenous for induction. Intervention 2: The thiopental group thiopental 4 mg /kg Intravenous for induction. Intervention 3: The thiopental and p
Treatment - Drugs
In propofol group, propofol 2 mg /kg Intravenous for induction
The thiopental group thiopental 4 mg /kg Intravenous for induction
The thiopental and propofol combined group propofol 1 mg /kg , thiopental 2 mg /kg Intravenous for induction

Sponsors

Birjand University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Inclusion criteria: ASA Class 1 and 2; candidate for elective cesarean section; fetus is normal and full term. Exclusion criteria: drug use by the mother; prolonged surgery; fetal abnormalities

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Apgar score. Timepoint: First and fifth minute Apgar score. Method of measurement: Apgar test.;Blood pressure. Timepoint: before induction of anesthesia, after intubation for 12 minutes once every 3 minutes. Method of measurement: Blood pressure device.;Pulse. Timepoint: before induction of anesthesia, after intubation for 12 minutes once every 3 minutes. Method of measurement: Monitoring device.;Oxygen saturation. Timepoint: before induction of anesthesia, after intubation for 12 minutes once every 3 minutes. Method of measurement: Pulse oximeter.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMaryam Tolyat

Birjand University of Medical Sciences

tolyatm@yahoo.com+98 56 3239 5453

Outcome results

None listed

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