The evaluation of the effect of administration of ketofol on hypotension due to regional anesthesia in cesarean section

The evaluation of the effect of infusion of ketofol on hypotension due to spinal anesthesia in cesarean section

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT201509282963N23

Enrollment

Registered

2016-02-23

Start date

2015-10-13

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

ketofol. Anaesthetic, unspecified

Interventions

Intervention 1: infusion of ketofol 1/10(infusion of 15 ml in 1 hour)or during surgery in intervention group. Intervention 2: infusion of normal saline( 15 ml/h) during surgery in placebo group.

Treatment - Drugs

infusion of ketofol 1/10(infusion of 15 ml in 1 hour)or during surgery in intervention group

infusion of normal saline( 15 ml/h) during surgery in placebo group

Eligibility

Sex/Gender

Female

Age

18 Years to 40 Years

Inclusion criteria

Inclusion criteria: inclusion criteria:18-35 years old women with term pregnancy ? American Society of Anesthesia (ASA) physical status I ? non- emergency repeated cesarean delivery ?spinal anesthesia. exclusion criteria: BMI>35 ; chronic hypertension; placenta previa; placenta acreta; gestational age <28 weeks; polyhydroamnious.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Hemodynamic variables. Timepoint: every 3 min during the surgery. Method of measurement: monitoring.	—

Secondary

Measure	Time frame
Level of sedation. Timepoint: every 15 min during the surgery. Method of measurement: Ramsay score.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Shekoufeh Behdad

Shahid Sadoughi University of Medical Sciences

behdad90@gmail.com+98 35 3822 4101

Outcome results

None listed

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