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Effect of Pre-loading of Colloid-Crystaloid Combination on Maternal Hemodynamic Status Following Spinal Anesthesia for Cesarean Delivery

Effect of Pre-loading of Colloid-Crystaloid Combination on Maternal Hemodynamic Status Following Spinal Anesthesia for Cesarean Delivery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20110712007013N22
Enrollment
70
Registered
2019-06-16
Start date
2018-10-23
Completion date
Unknown
Last updated
2019-08-26

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

Conditions

Effect of Pre-loading of Colloid-Crystaloid Combination on Maternal Hemodynamic Status Following Spinal Anesthesia for Cesarean Delivery. Other complications of spinal and epidural anaesthesia during labour and delivery

Interventions

Intervention 1: Intervention group: The study group (35 cases (8ml / kg colloid + crystalloid solution (ringer) with equal volume. Intervention 2: Control group: The placebo group (35 cases) received

Sponsors

Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: The desire to participate in the study Elective cesarean candidate A candidate for spinal anesthesia ages 18-40 Class I ASA grading Single term pregnancy

Exclusion criteria

Exclusion criteria: - multiple pregnancy - Weight over 100 kg and height less than 150 cm History of systemic diseases (cardiovascular, liver, kidney, etc.)- History of mental disorder Contraindications for spinal anesthesia A history of allergy to Boyoukain Emergency cesarean section fetal problems(IUGR, meconium excretion, asyphexy ...) Hypertension during pregnancy Starch allergy

Design outcomes

Primary

MeasureTime frame
Severity of hypotension. Timepoint: Basic times, every two minutes to 10 minutes, then minutes 15, 20, 30. 45 and 60 and the end. Method of measurement: Automatic pressure gauge.

Secondary

MeasureTime frame
Severity of Changes in Mother's Heart Rate. Timepoint: Basic times, every two minutes to 10 minutes, then minutes 15, 20, 30. 45 and 60 and the end. Method of measurement: pulseoximetry.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Simin Atashkhoyi

Tabriz University of Medical Sciences

satashkhoyi@gmail.com+98 41 3553 9161

Outcome results

None listed

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