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NCT04126382

LISA vs INSURE in the Treatment of Respiratory Distress Syndrome in Preterm Infants

Status unknown Phase 2 Last updated 15 October 2019
What this trial tests

Phase 2 trial testing Intubate-Surfactant-Extubate(INSURE) in Preterm Infants in 200 participants. Status unknown.

Timeline
1 January 2020
Primary endpoint
31 December 2024
31 December 2024

Quick facts

Lead sponsorAnhui Provincial Hospital
PhasePhase 2
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment200
Start date1 January 2020
Primary completion31 December 2024
Estimated completion31 December 2024

Drugs / interventions tested

Conditions studied

Sponsor

Anhui Provincial Hospital

Who can join

Adults 25 Weeks to 32 Weeks, any sex, with Preterm Infants. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

To evaluate the efficacy of less invasive surfactant administration(LISA )technique in the treatment of neonatal respiratory distress syndrome(NRDS) by comparing with the traditional Intubate-Surfactant-Extubate(INSURE) technique.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Preterm Infants

Currently open trials in the same condition.

Other Anhui Provincial Hospital trials

Trials by the same sponsor.

Verify against primary sources

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/NCT04126382.

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