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Comparison of crystalloid with colloid in sensory level induced by spinal anesthesia in cesarean section

A randomized study to compare the sensory levels of spinal anesthesia for elective cesarean section using crystalloid versus Voluven solution

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20120910010800N10
Enrollment
120
Registered
2023-01-15
Start date
2023-02-04
Completion date
Unknown
Last updated
2023-02-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hypotension due to drugs. Hypotension due to drugs

Interventions

Intervention 1: Intervention group: Normal saline group: Within thirty minutes before spinal anesthesia, the anesthesiologist will inject 10 ml/kg of 0.9% sodium chloride solution intravenously to the

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: singleton pregnancy Elective cesarean section Gestational age more than 36 weeks Height more than 150 and less than 175 cm Body mass index less than 35 kg/m2 Consent to study

Exclusion criteria

Exclusion criteria: Sensitivity to local anesthetics

Design outcomes

Primary

MeasureTime frame
The sensory level obtained after spinal anesthesia. Timepoint: Every 5 to 30 minutes after spinal anesthesia and then at 60 and 90 minutes. Method of measurement: The sensory level will be assessed along the midline of the abdomen from T12 towards the patient's head with a blunt needle.

Secondary

MeasureTime frame
Hypotension after spinal anesthesia. Timepoint: Throughout the operation in 5-minute intervals to 30 minutes, then in 10-minute intervals until the end of the operation. Method of measurement: Standard blood pressure monitoring.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDariush Abtahi

Shahid Beheshti University of Medical Sciences

d.abtahi@sbmu.ac.ir+98 21 2263 2611

Outcome results

None listed

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