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the prediction of hypotension according to change of ANI

Prediction of hypotension based on ANI (analgesia nociception index) change during cesarean section under combined spinal-epidural anesthesia

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CRIS
Registry ID
KCT0009333
Enrollment
55
Registered
2024-04-12
Start date
2024-07-28
Completion date
Unknown
Last updated
2024-12-09

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

Conditions

None listed

Interventions

None listed

Sponsors

Samsung Medical Center
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: - full term pregnancy (more than amenorrhea 37wks ) - American society of anesthesiologist physical status 1 2 - pregnant women undergoing elective cesarean section under combined spinal epidural anesthesia

Exclusion criteria

Exclusion criteria: -Fetal abnormality - Those taking drugs that may affect the sympathetic nervous system: beta blockers, anticholinergic drugs, anti-anxiety drugs, antidepressants, sedatives - arrhythmia - Multiple pregnancy - ANI measurement is not possible (those who have skin damage at the sensor attachment site or have a history of allergies when using adhesive electrodes) - who do not understand the study content or do not agree to participate in the study

Design outcomes

Primary

MeasureTime frame
hypotension—

Secondary

MeasureTime frame
ANI variables;hemodynamic varaibles;Hypotension related variables;vasopressor dosage;Apgar score and cord pH of neonate;level of spinal epidural anesthesia—

Countries

Korea, Republic of

Contacts

Public ContactYu Jeong Bang

Samsung Medical Center

gagreflex.bang@gmail.com+82-2-3410-2486

Outcome results

None listed

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