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Safety of Phenylephrine in Antihypotensive Treatment during Spinal Anesthesia for Cesarean Section

Safety of Phenylephrine in Antihypotensive Treatment during Spinal Anesthesia for Cesarean Section

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
TCTR
Registry ID
TCTR20141017001
Enrollment
Unknown
Registered
2014-10-17
Start date
2014-07-07
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Phenylephrine&#45

Interventions

Treatment

Sponsors

Graduate school Chulalongkorn university
Lead Sponsor
9oth Anniversary of Chulalongkorn University Scholarship
Collaborator

Eligibility

Sex/Gender
Female
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: - ASA I,II - Age greater than or equal 18 years old. - Singleton baby. - Gestational age greater than or equal to 37 weeks

Exclusion criteria

Exclusion criteria: Chronic hypertension, gestational hypertension or preeclampsia. - Cardiovascular disease (ischemic heart disease, valvular heart disease, cardiac defect) or cerebrovascular disease (stroke, cerebral aneurysm, cerebral arteriovenous malformation) - Complicated obstetrics (abruptio placenta, placenta previa) - Known fetal abnormalities (intrauterine growth retardation(IUGR), fetal cardiac disease) - History use of monoamine oxidase inhibitor(MAOI). - History use of other drugs that prolonged heart conduction(PR or QT interval) - Contraindications to spinal anesthesia (coagulopathy, intracranial space occupying lesion or patient refusal)

Design outcomes

Primary

MeasureTime frame
Incidences of phenylephrine-induced bradycardia in treatment of spinal anesthesia-induced hypotensio End of study Percentage

Secondary

MeasureTime frame
Association of pretherapeutic heart rate and phenylephrine-induced bradycardia End of study Relative risk,The optimal cut-point of heart rate that safe for using phenylephrine End of study Multivariable logistic regression,The incidences of severe adverse events End of study Percentage

Countries

Thailand

Contacts

Public ContactRatikorn Anusorntanawat

Chaoprayayomraj hospital

netanesth@hotmail.com+66819424915

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026