Trials / Completed
CompletedNCT01033526
Symptomatic Treatment of Common Cold Symptoms
A Two-arm, Multicenter, Randomized, Double-blind, Single Dose Placebo-controlled Parallel Groups Study Evaluating Efficacy and Tolerability of 800 mg Acetylsalicylic Acid (Aspirina® C) in Adult Patients With a Common Cold During a Two Hour in Patient Phase; and a Follow-up Period of Five Days of Home Treatment as Required
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 388 (actual)
- Sponsor
- Bayer · Industry
- Sex
- All
- Age
- 18 Years – 65 Years
- Healthy volunteers
- Not accepted
Summary
A two-arm, multicenter, randomized, double-blind, single dose placebo-controlled parallel groups study evaluating efficacy and tolerability of 800 mg Acetylsalicylic Acid (Aspirina C) in adult patients with a common cold during a two hour in patient phase; and a follow-up period of five days of home treatment as required.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Aspirin (Acetylsalicylic acid, BAYE4465) | 1-2 tablets Acetylsalicylic Acid 400 mg (in combination with Ascorbic Acid 240 mg) as needed every 4-6 hours over a maximum of 5 days |
| DRUG | Placebo | 1-2 tablets matching Placebo as needed every 4-6 hours over a maximum of 5 days |
Timeline
- Start date
- 2005-10-01
- Completion
- 2007-06-01
- First posted
- 2009-12-16
- Last updated
- 2009-12-16
Locations
28 sites across 1 country: Italy
Source: ClinicalTrials.gov record NCT01033526. Inclusion in this directory is not an endorsement.