Clinical trial

Effects of Mometasone Furoate Dry Powder Inhaler, Fluticasone Propionate, and…

NCT00394355 · Organon and Co, Industry · Completed

Key facts

NCT number NCT00394355
Title Effects of Mometasone Furoate Dry Powder Inhaler, Fluticasone Propionate, and Montelukast on Bone Mineral Density in Asthmatics (Study P03418)
Official title Comparative Study of the Effect of Two Doses of Mometasone Furoate Dry Powder Inhaler 200 mcg and 400 mcg QD PM, Fluticasone Propionate 250 mcg BID, and Montelukast 10 mg QD PM, on Bone Mineral Density in Adults With Asthma
Lead sponsor Organon and Co, Industry
Status Completed
Phase Phase 4
Study type Interventional
Conditions Asthma
Intervention type Drug
Interventions mometasone furoate dry powder inhaler, fluticasone propionate hydrofluoroalkane (HFA), montelukast
Enrollment 566
Start date Sep 1, 2006
Primary completion Oct 1, 2009
Completion Oct 1, 2009
First posted Nov 1, 2006
Last update posted May 22, 2024

At a glance

  • Yes Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

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