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EVALUATION OF PULSE OXYMETER PARAMETER TO PREDICT REQUIREMENT OF DRUGS TO INCREASE BLOOD PRESSURE IN PATIENTS WITH SEPSIS

EVALUATION OF PERFUSION INDEX AS A PREDICTOR OF VASOPRESSOR REQUIREMENT IN PATIENTS WITH SEPSIS - A PROSPECTIVE OBSERVATIONAL STUDY - PerfPredict

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2023/02/049572
Enrollment
35
Registered
2023-02-09
Start date
Unknown
Completion date
Unknown
Last updated
2023-03-06

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

Conditions

Health Condition 1: A419- Sepsis, unspecified organism

Interventions

Intervention1: Nil: Nil Control Intervention1: Nil: Nil

Sponsors

Indraprastha Apollo Hospitals
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Age > 18 years Clinically suspected sepsis Adequate Fluid Resuscitation (30ml/kg)

Exclusion criteria

Exclusion criteria: Age Pregnant Females inadequate fluid resuscitation ( Already receiving vasopressor therapy

Design outcomes

Primary

MeasureTime frame
Compare perfusion index to arterial lactate levels at T0 and T6 hours as predictor of vasopressor requirement in first 24 hourTimepoint: Compare perfusion index to arterial lactate levels at T0 and T6 hours as predictor of vasopressor requirement in first 24 hour—

Secondary

MeasureTime frame
final outcome of patients with sepsis (Discharged / Death)Timepoint: 0-28 days—

Countries

India

Contacts

Public ContactDr Jaydeep Narendrabhai Anadkat

Indraprastha Apollo Hospitals

kansalsudha08@gmail.com9810399558

Outcome results

None listed

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