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Outcomes of elevated lactate levels in patients admitted to intensive care units

An Observational Study on outcomes of hyperlactatemia on admission in critically ill patients. - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2025/07/090636
Enrollment
100
Registered
2025-07-10
Start date
Unknown
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

Health Condition 1: - Health Condition 2: R740- Nonspecific elevation of levels oftransaminase and lactic acid dehydrogenase [LDH]

Interventions

Intervention1: Nil: Nil Intervention2: Nil: Nil Intervention3: Nil: Nil Intervention4: Nil: Nil

Sponsors

SRI RAMACHANDRA INSTITUTE OF HIGHER EDUCATION AND RESEARCH
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: patient with elevated lactate levels. clinical conditions associated with tissue hypoxia and systemic disease. all consecutive critically ill adult age above 19 years.

Exclusion criteria

Exclusion criteria: neonates and paediatric patients. incomplete records or missing data.

Design outcomes

Primary

MeasureTime frame
Development of multi organ dysfunction syndrome(MODS) lactate clearance and its association with clinical deterioration factors enchance lactate clearance at 24 hours and at 48 hours abg serum lactate apache 2 score and sofa scoreTimepoint: 8weeks—

Secondary

MeasureTime frame
length of ICU stay need for organ suport(mechanical ventilation, vasopressors) hospital mortalityTimepoint: 10 months—

Countries

India

Contacts

Public ContactDr Renuka MK

Sri Ramachandra Institute of Higher Education and Reasearch

sailajaroop@gmail.com9600159482

Outcome results

None listed

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