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NCT00030121

A Phase II, Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Dose-Ranging Evaluation of the Safety and Efficacy of Carperitide Infusion in Patients With ARDS

Completed Phase 2 Last updated 19 February 2008
What this trial tests

Phase 2 trial testing recombinant human atrial natriuretic polypeptide in Respiratory Distress Syndrome. Completed.

Timeline
1 December 1999

Quick facts

Lead sponsorSuntory Pharmaceutical
PhasePhase 2
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposetreatment
Start date1 December 1999

Drugs / interventions tested

Conditions studied

Sponsor

Suntory Pharmaceutical — full company profile →

Who can join

18 and older, any sex, with Respiratory Distress Syndrome. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this study is to determine whether Carperitide is safe and effective in the management of Acute Respiratory Distress Syndrome (ARDS).

Publications & conference data

2 peer-reviewed publications reference this trial (live from Europe PMC):

  1. What every intensivist should know about acute respiratory distress syndrome and diffuse alveolar damage.
    Rios F, Iscar T, Cardinal-Fernández P. · · 2017 · cited 17× · PMID 28977098 · DOI 10.5935/0103-507x.20170044
  2. Do Nonventilatory Strategies for Acute Lung Injury and ARDS Work?
    · 2010

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Other recruiting trials for Respiratory Distress Syndrome

Currently open trials in the same condition.

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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/NCT00030121.

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