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Completed trials with posted results — search by concept, filter by the parameters that matter at the bedside.

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12,372 trials

Phase 3 N=733 Study to Evaluate the 24-Hour Pulmonary Function Profile of Fluticasone Furoate (FF) /GW642444 (Vilanterol) (VI) Inhalation Powder 100/25mcg Once Daily Compared With Fluticasone Propionate/Salmeterol Inhalation Powder 250/50mcg Twice Daily in Subjects With Chronic Obstructive Pulmonary Disease

Pulmonary Disease, Chronic Obstructive
Primary: Change From Baseline Trough in 24-hour Weighted-mean FEV1 on Treatment Day 84 — 0.094; 0.174 Liters — p=<0.001
GlaxoSmithKline Results Jul 2013 2.1% serious AE View details

Phase 3 N=702 A Study to Evaluate the 24 Hour Spirometric Effect (FEV1) of Fluticasone Furoate/Vilanterol Inhalation Powder (100mcg Fluticasone Furoate (FF)/25mcg Vilanterol (VI)) Compared With Salmeterol/Fluticasone Propionate Inhalation Powder (50mcg Salmeterol/500mcg Fluticasone Propionate (FP))

Pulmonary Disease, Chronic Obstructive
Primary: Change From Baseline Trough in 24-hour Weighted-mean FEV1 on Treatment Day 84 — 0.108; 0.130 Liters — p=0.282
GlaxoSmithKline Results Jul 2013 1.7% serious AE View details

Phase 3 N=65 In Situ Caries Model of Fluoride Toothpastes

Caries
Primary: Percent Surface Microhardness (SMH) Recovery of Enamel Specimens Exposed to NaF Toothpaste (1426ppmF) and AmF Toothpaste (1400ppmF) — 38.05; 41.06 Percentage SMHR…
GlaxoSmithKline Results Jul 2013 0.0% serious AE View details