A Phase 3 interventional study of Acetylsalicylic acid (Aspirin, BAYE4465) & Lidocain and Acetylsalicylic Acid (Aspirin, BAYE4465) in Common Cold, Pharyngitis and Tonsillitis, sponsored by Bayer. Completed at 19 sites in 2 countries. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2023-10-18.
Sponsored by Bayer · Phase 3, Interventional, and Treatment
The purpose of this study is to investigate the analgesic efficacy of a single dose of a fixed combination of 500 mg Aspirin (Acetylsalicylic Acid) and 4 mg Lidocaine in adult patients with sore throat associated with a common cold in comparison to a single treatment with 500 mg Aspirin or 4 mg Lidocaine alone as well a Placebo (treatment without any active ingredient). The combination of Aspirin and Lidocaine in a single lozenge is expected to provide relief from sore throat pain by sequential action. A very fast inset of action will be achieved by the locally acting Lidocaine and a long duration of action will be achieved by the systemically acting Aspirin.
219 studies on the registry are indexed under Common Cold; 23 are open to participants now.
This study's enrollment of 1,088 is above the median of 150 across 184 interventional studies indexed under Common Cold.
Browse Common Cold studies →Bayer is the lead sponsor of 1,674 studies on the registry; 51 are open to participants now.
Of its 214 completed or terminated interventional studies of FDA-regulated products, 132 (62%) have results posted.
Counted across the registry records on this site, refreshed daily.
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Exclusion Criteria:
Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
An allergy, or another reaction of the immune system, to a substance. “Hypersensitivity to the study drug” means a known allergic reaction to it — not every side effect a medicine can have.
Hypersensitivity
An allergy, or another reaction of the immune system, to a substance. “Hypersensitivity to the study drug” means a known allergic reaction to it — not every side effect a medicine can have.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Drug: Acetylsalicylic acid (Aspirin, BAYE4465) & Lidocain
Drug: Acetylsalicylic Acid (Aspirin, BAYE4465)
Drug: Lidocain
Drug: Placebo
Single oral application of a fixed combination of Aspirin and Lidocain (as one lozenge)
Single oral application of Aspirin (as lozenge)
Single oral application of Lidocain (as lozenge)
Single oral application of Placebo (as lozenge)
Sum of pain intensity differences SPID
Time frame: 120 minutes
Pain intensity difference to baseline (PID12 min)
Time frame: 12 minutes
Pain intensity difference to baseline (PID120 min)
Time frame: 120 minutes
Pain intensity difference to baseline (PID)
Time frame: 3, 6, 12, 18, 24, 30, 40, 50, 60, 75, 90, 105, 120, 150, 180, 210 and 240 minutes post dose
Total pain relief to baseline (TOTPAR)
Time frame: 3, 6, 12, 18, 24, 30, 40, 50, 60, 75, 90, 105, 120, 150, 180, 210 and 240 minutes post dose
Symptoms of common cold (headache, sinus pressure/pain, feverish discomfort, muscle aches and pain)
Time frame: 60, 120, 180, and 240 minutes post dose
Overall assessment of treatment
Time frame: 240 minutes
Assessment of safety and tolerability
Time frame: 240 minutes
Ran from Nov 2004 to primary completion in May 2005, 5 months.
Of 17 phase 3 interventional studies under Common Cold, half reached primary completion within 7 months of starting (the median), counting those still running; a quarter within 5 and three quarters within 16. This study's 5 months is below that.
How these figures are worked out, and which studies are left out of them.
This study is completed, as verified in Oct 2023. You cannot join it, but the record below documents what was studied.
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Studies of the drug tested here: Aspirin