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Human Clinical Study: Assessment of Zicam Cold Remedy RapidMelts

Human Clinical Study: Assessment of Zicam Cold Remedy RapidMelts

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
EU CTR
Registry ID
EUCTR2005-004641-34-GB
Enrollment
200
Registered
2005-12-05
Start date
2006-02-07
Completion date
Unknown
Last updated
2012-04-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

to shorten the duration, reduce the number and decrease the sevity of common cold symptoms in otherwise healthy human adult volunteers

Interventions

Product Name: Zicam RapidMelts Product Code: n/a Pharmaceutical Form: Tablet INN or Proposed INN: Zinc acetate USP CAS Number: 5970-45-6 Current Sponsor code: - Other descriptive name: - Concentration

Sponsors

Matrixx Initiatives Inc
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Onset of common cold symptoms within 24 hours preceding pre-enrolment screening.Male and female volunteers 18 years of age and above.In good general health other than the common cold. Are the trial subjects under 18? no Number of subjects for this age range: F.1.2 Adults (18-64 years) yes F.1.2.1 Number of subjects for this age range F.1.3 Elderly (>=65 years) no F.1.3.1 Number of subjects for this age range

Exclusion criteria

Exclusion criteria: Cold symptoms for more than 24 hours at time of enrolment.History of perennial allergic rhinitis, asthma or any other chronic respiratory disease.Prior history of adverse reaction to zinc, calcium or any of the inactive ingredients of Zicam RapidMelts tablets.

Design outcomes

Primary

MeasureTime frame
Main Objective: Shorten the duration of common cold symptoms;Secondary Objective: Reduce the number of common cold symptoms2. Decrease the severity of common cold symptoms Decrease the severity of common cold symptoms;Primary end point(s): End of common cold symptoms

Countries

United Kingdom

Outcome results

None listed

Source: EU CTR (via WHO ICTRP) · Data processed: Feb 4, 2026