Placebo and Active Controlled Study to Assess Efficacy and Tolerability of Aspirin Plus Pseudoephedrine

Completed · Phase 3 · Has a placebo group

Conditions studied: Common Cold, Pharyngitis

In brief

The purpose of this study is compare efficacy and tolerability of a fixed combination, containing 500 mg Acetylsalicylic acid and 30 mg Pseudoephedrine, in comparison to its single components in patients with sore throat and nasal congestion.

Key facts

Study ID

NCT01062360

Run by

Bayer

People needed

1016

Starts

2005-12-23

Expected to finish

2007-05-14

Last updated by the study team

2017-09-01

Who can join

Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.

Where it is running

• Study site — New York, New York, United States
• Study site — Alassio, Italy
• Study site — Albenga, Italy
• Study site — Arenzano, Italy
• Study site — Civitella Marittima, Italy
• Study site — Follonica, Italy
• Study site — Genova, Italy
• Study site — Genova, Italy
• Study site — Genova, Italy
• Study site — Genova, Italy
• Study site — Genova, Italy
• Study site — Genova, Italy
• Study site — Genova, Italy
• Study site — Genova, Italy
• Study site — Genova, Italy
• Study site — Genova, Italy
• Study site — Grosseto, Italy
• Study site — Grossetto, Italy
• Study site — Isola del Cantone, Italy
• Study site — Loano, Italy
• Study site — Masone, Italy
• Study site — Orbetello, Italy
• Study site — Pegli, Italy
• Study site — Quiliano, Italy
• Study site — New York, New York, United States

Full record on ClinicalTrials.gov

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