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efficacy of administration crystalloid fluid in hypotansion in spinal anesthesia

Assessment of efficacy of administration crystalloid fluid and no administration crystalloid fluid in prevention of spinal anesthesia-induced hemodynamic changes in pregnant women candidate for elective caesarean section

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2013030212642N1
Enrollment
74
Registered
2013-03-25
Start date
2012-08-22
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

elective cesarean section. delivery by elective cesarean section

Interventions

Intervention 1: for the case group, ringer lactate iv fluid in the dose of 15cc/kg will administer 10-20min before the procedure of CS. Intervention 2: no administered of iv fluid of ringer lactat.
Prevention
for the case group, ringer lactate iv fluid in the dose of 15cc/kg will administer 10-20min before the procedure of CS
no administered of iv fluid of ringer lactat

Sponsors

Arak Univercity Of Medicak Science
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
15 Years to 45 Years

Inclusion criteria

Inclusion criteria: The inclusion criteria for the study Women 15 to 45 years; absence of systemic disease; no current history of substance abuse, no current history of drug use; a suitable level of anesthesia The exclusion criteria for the study All patients entered in the study, women younger than 15 years or more than 45 year; women with systemic disease, heart - lung, kidney, glandular or metabolic disease, blood pressure, primary or secondary, pre-eclampsia or eclampsia, mental illness, morbid obesity, pregnancy the multiple and polyhydroamnious removed; All patients entered in the study, women with a history of current use of alcohol, cigarettes and drugs, opioids and beta blockers or agonist drug consumers are excluded; the lack of a suitable anesthetic level (level T4) after the first step for spinal anesthesia; changes before and during surgical anesthesia for any reason

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Maternal blood pressure. Timepoint: After inducing spinal anesthesia, the maternal blood pressure will collect every 3 minutes till the baby delivery and every 15 minutes till the end of the surgery and recovery of the sense of the lower extremities. Method of measurement: mmhg.

Secondary

MeasureTime frame
Neonatal apgar. Timepoint: 1th, 5th, 10th after birth. Method of measurement: The Apgar Scoring System.;Maternal heart rate. Timepoint: After inducing spinal anesthesia, heart beats will collect every 3 minutes till the baby delivery and every 15 minutes till the end of the surgery and recovery of the sense of the lower extremities. Method of measurement: beat in minute.

Countries

Iran (Islamic Republic of)

Outcome results

None listed

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