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Clinical Trials/CTRI/2024/07/071249
CTRI/2024/07/071249
Not yet recruiting
Not Applicable

Evaluation of real time perfusion index as an early indicator for hypotension in a lower segment caesarean section observational study

Nanthitha Sri1 site in 1 country109 target enrollmentStarted: August 4, 2024Last updated:
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Overview

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Nanthitha Sri
Enrollment
109
Locations
1
Primary Endpoint
Perfusion Index and Perfusion ratio to predict hypotension early when compared it with NIBP
OverviewStudy DesignEligibility CriteriaOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Overview

Brief Summary

Hypotension can be monitored non-invasively by the NIBP. For real-time measurement of NIBP, Invasive measurements can be done using arterial blood pressure, but they are not cost-efficient. In modern medicine, the perfusion index is faster at predicting hypotension when compared with non-invasive blood pressure measurement.

Study Design

Study Type
Observational

Eligibility Criteria

Ages
18.00 Year(s) to 45.00 Year(s) (—)
Sex
Female

Inclusion Criteria

  • •Parturient undergoing elective LSCS Patients with ASA â…¡ and â…¢ Grading.

Exclusion Criteria

  • •LSCS done under general anaesthesia Twin gestation Pregnancy induced hypertension Pre-eclampsia Emergency LSCS Chronic hypertension.

Outcomes

Primary Outcomes

Perfusion Index and Perfusion ratio to predict hypotension early when compared it with NIBP

Time Frame: 8 months

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Nanthitha Sri
Sponsor Class
Other [self]
Responsible Party
Principal Investigator
Principal Investigator

Nanthitha Sri

Manipal college of health professions MAHE Manipal

Study Sites (1)

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