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The evaluation of the effect of administration of dexamethasone on hemodynamic variables and hypotension due to regional anesthesia in the women undergoing cesarean section

The evaluation of the effect of intravenous dexamethasone on hemodynamic variables and post-spinal hypotension in the women undergoing cesarean section

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20100102002963N34
Enrollment
60
Registered
2022-01-23
Start date
2022-04-04
Completion date
Unknown
Last updated
2022-02-07

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

Conditions

Hemodynamic variables and hypotension after spinal anesthesia in the women undergoing cesarean section. Postprocedural hypotension

Interventions

Intervention 1: Intervention group: In this group, dexamethasone at a dose of eight mg equivalent to 2 ml is injected slow intravenously and once immediately before spinal anesthesia to eligible patie

Sponsors

Yazd University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 35 Years

Inclusion criteria

Inclusion criteria: 20-35 years old women with term pregnancy American Society of Anesthesia (ASA) physical status I non- emergency repeated cesarean delivery spinal anesthesia

Exclusion criteria

Exclusion criteria: BMI>35 chronic hypertension placenta previa placenta acreta gestational age <28 weeks Polyhydramnios

Design outcomes

Primary

MeasureTime frame
Systolic blood pressure. Timepoint: Before the injection of the study drug, immediately after the spinal anesthesia and then every three minutes until the birth of the baby and then every 5 minutes until the end of surgery, and every 15 minutes during recovery. Method of measurement: Using monitoring device.;Diastolic Blood Pressure. Timepoint: Before the injection of the study drug, immediately after the spinal anesthesia and then every three minutes until the birth of the baby and then every 5 minutes until the end of surgery, and every 15 minutes during recovery. Method of measurement: Using monitoring device.;Mean Arterial Pressure. Timepoint: Before the injection of the study drug, immediately after the spinal anesthesia and then every three minutes until the birth of the baby and then every 5 minutes until the end of surgery, and every 15 minutes during recovery. Method of measurement: Using monitoring device.;Heart Rate. Timepoint: Before the injection of the study drug, immediately after the spinal anesthesia and then every three minutes until the birth of the baby and then every 5 minutes until the end of surgery, and every 15 minutes during recovery. Method of measurement: Using monitoring device.;Drop in systolic blood pressure below 90 mm Hg. Timepoint: Before the injection of the study drug, immediately after the spinal anesthesia and then every three minutes until the birth of the baby and then every 5 minutes until the end of surgery, and every 15 minutes during recovery. Method of measurement: Using monitoring device.

Secondary

MeasureTime frame
Bradycardia(drop in heart rate below 50/ min). Timepoint: Before the injection of the study drug, immediately after the spinal anesthesia and then every three minutes until the birth of the baby and then every 5 minutes until the end of surgery, and every 15 minutes during recovery. Method of measurement: Using monitoring device.;Hyperglycemia( blood glucose more than 200mg/dl). Timepoint: In the recovery (one hour after operation). Method of measurement: using Glucometer.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Shekoufeh Behdad

Yazd University of Medical Sciences

drbehdad@ssu.ac.ir0098 35 8231932

Outcome results

None listed

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