Last updated: 11/04/2018 10:27:30

The effect of a nutritional supplement on post prandial glucose and lipids in an adult population

GSK study ID
RH01948
Clinicaltrials.gov ID
Not applicable
EudraCT ID
Not applicable
EU CT Number
Not applicable
Trial status
Finalized
Finalized
Overview
Eligibility
Locations
Study documents
Results summary
Plain language summaries
Additional information

Trial overview

Official title: Contac Nasal Spray Questionnaire
Trial description: As Contac nasal spray was approved as a switch over-to-counter, it was mandatory to carry out post marketing surveillance (PMS) for a certain period and to report its result to PMDA. With this purpose, GSK has selected stores to participate in PMS of ‘Contac Nasal Spray’, and will be asking customers to fill in the questionnaire regarding efficacy and frequency of adverse effects, etc, in order to comprehend its actual usage in the market. In this way, collected information will be utilized to help develop products that ensure further safety and satisfaction of the consumers. The consumers will bring the filled questionnaire after using the nasal spray to the store from where it was purchased.
Primary purpose:
Not applicable
Trial design:
Not applicable
Masking:
Not applicable
Allocation:
Not applicable
Primary outcomes:

Filled questionnaire form after using Contac Nasal Spray

Timeframe: 37 Months

Secondary outcomes:
Not applicable
Interventions:
Drug: CONTAC® Nasal spray
Enrollment:
478
Observational study model:
Other
Primary completion date:
2013-01-12
Time perspective:
Prospective
Clinical publications:
Not applicable
Medical condition
Seasonal Allergic Rhinitis, Nasal Congestion
Product
Not applicable
Collaborators
Not applicable
Study date(s)
February 2011 to December 2013
Type
Observational
Phase
Not applicable

Participation criteria

Sex
Female & Male
Age
18 - 65 Year
Accepts healthy volunteers
none
  • Participants purchasing Contac Nasal Spray aged 18-65 years.
  • N/A

Trial location(s)

No location data available.

Study documents

No study documents available.

Results overview

No study documents available

Recruitment status
Finalized
Actual primary completion date
2013-01-12
Actual study completion date
2013-01-12

Plain language summaries

Not applicable. GSK’s transparency policy provides for Plain Language Summaries for Interventional studies.

Additional information about the trial

Not applicable
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