predelivery conscious sedation in mothers under cesarean delivery with spinal anesthesia

Predelivery conscious sedation of mothers under cesarean delivery with spinal anesthesia by Thiopantal (0.25,0/5,0.75 mg/kg)

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

IRCT

Registry ID

IRCT2014011116162N1

Enrollment

240

Registered

2014-07-12

Start date

2014-05-14

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

The rate of conscious sedation. -Delivery by elective caesarean section

Interventions

Intervention 1: Intervention in group1: 0.25mg/kg/IV Thiopental Na is injected. Intervention 2: Intervention in group2: 0.5 mg/kg/IV Thiopental Na is injected. Intervention 3: Intervention in group3

Treatment - Drugs

Placebo

Intervention in group1: 0.25mg/kg/IV Thiopental Na is injected

Intervention in group2: 0.5 mg/kg/IV Thiopental Na is injected

Intervention in group3: 0.75 mg/kg/IV Thiopental Na is injected

Intervention in control group: 1.5 cc/IV Normal saline is injected

Eligibility

Sex/Gender

Female

Age

20 Years to 30 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: nulligravid women with a normal pregnancy and an The American Society of Anesthesiologists (ASA) physical status I, II. Exclusion criteria:patients having bleeding or suspicious disorders, abnormality in vertebral column, infection in back, liver or kidney disease, taking anticoagulant and patient with hypertension of pregnancy or preeclampsia.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Sedation. Timepoint: After surgery. Method of measurement: Questionnaire.	—

Secondary

Measure	Time frame
Oversadation. Timepoint: During surgery. Method of measurement: observation.;Number of infant's APGAR. Timepoint: After surgery. Method of measurement: Observation.;Infant blood PH. Timepoint: after sergury. Method of measurement: PH metere.;Respiratory arrest. Timepoint: during surgery. Method of measurement: observation.;Nausea and vomiting. Timepoint: during surguey. Method of measurement: observation.;Amnesia. Timepoint: after sergury. Method of measurement: observation.;Drop in blood pressure. Timepoint: during surgery. Method of measurement: measuring by Pressure set.	—

Measure

Time frame

Oversadation. Timepoint: During surgery. Method of measurement: observation.;Number of infant's APGAR. Timepoint: After surgery. Method of measurement: Observation.;Infant blood PH. Timepoint: after sergury. Method of measurement: PH metere.;Respiratory arrest. Timepoint: during surgery. Method of measurement: observation.;Nausea and vomiting. Timepoint: during surguey. Method of measurement: observation.;Amnesia. Timepoint: after sergury. Method of measurement: observation.;Drop in blood pressure. Timepoint: during surgery. Method of measurement: measuring by Pressure set.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactMasomeh Nataj Majd

Tehran University of Medical Sciences

mnataj54@yahoo.com+98 21 7771 9922

Outcome results

None listed

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