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Effects of two different dosages of Remifentanil at Induction of General Anesthesia for Cesarean Delivery

Maternal and Neonatal Effects of two different dosages of Remifentanil at Induction of General Anesthesia for Cesarean Delivery

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201105162883N2
Enrollment
90
Registered
2011-05-26
Start date
2009-12-30
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

Complications of anaesthesia during labour and delivery. Complications of anaesthesia during labour and delivery

Interventions

Intervention 1: Control group: normal saline will be infused by the same volume and rate. Intervention 2: Intervention group A: infusion of remifentanil 0.2µg/kg/min. Intervention 3: Intervention grou
Placebo
Treatment - Drugs
Control group: normal saline will be infused by the same volume and rate
Intervention group A: infusion of remifentanil 0.2µg/kg/min
Intervention group B: infusion of remifentanil 0.1µg/kg/min

Sponsors

Research Vice Chancellor of Mazandaran University of Medical Sciences and Health Services
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: women aged 18-35 years with American Society of Anesthesiologist physical status class I- II, candidate for elective cesarean section under general anesthesia Exclusion criteria: associated disease such as preeclampsia, hypertension, history of difficult intubation, cardiovascular or respiratory disorders, diabetes

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Blood pressure of the mothers. Timepoint: Before infusion and just before and after tracheal intubation and 5 min after that-. Method of measurement: BP Monitoring.;Heart rates of the mothers. Timepoint: Before infusion and just before and after tracheal intubation and 5 min after that. Method of measurement: ECG Monitor and pulseoxymetry.;Apgar score of neonates. Timepoint: At the first and 5th minutes after birth. Method of measurement: by the pediatrician coinvestigator.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Mohammadreza Habibi

Mazandaran University of Medical Sciences

MHabibi@mazums.ac.ir mohammadrezahabibi@gmail.com+98 15 1226 1704

Outcome results

None listed

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