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NCT05924230

Dose Responsive Study of Ringer's Lactate Solution in Prevention of Post-induction Hypotension

Status unknown NA Last updated 29 June 2023
What this trial tests

NA trial testing RL 10ml/kg in Post Induction Hypotension in 100 participants. Status unknown.

Timeline
1 April 2023
Primary endpoint
30 June 2024
31 August 2024

Quick facts

Lead sponsorTata Main Hospital
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposetreatment
Enrollment100
Start date1 April 2023
Primary completion30 June 2024
Estimated completion31 August 2024
Sites1 location across India

Drugs / interventions tested

Conditions studied

Sponsor

Tata Main Hospital

Who can join

Adults 18 to 65, any sex, with Post Induction Hypotension. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

To assess the dose responsiveness of ringer lactate solution in prevention of post-induction hypotension predicted by Ultrasound guided Inferior Vena Cava diameter in patients receiving General anesthesia. OBJECTIVES Primary - To find the optimum preloading dosage of Ringer Lactate to prevent post induction hypotension. Secondary - To find the predictive incidence of Post-induction hypotension according to age, gender, type of surgery and comorbidities.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other Tata Main Hospital trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05924230.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing