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
Study complete
Study complete
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:
Enrollment:
478
Primary completion date:
2013-01-12
Observational study model:
Other
Time perspective:
Prospective
Clinical publications:
Not applicable
- Participants purchasing Contac Nasal Spray aged 18-65 years.
- N/A
Inclusion and exclusion criteria
Inclusion criteria:
- Participants purchasing Contac Nasal Spray aged 18-65 years.
Exclusion criteria:
- N/A
Trial location(s)
This study does not involve prospective enrollment of participants.
Study documents
No study documents available.
Results overview
No study documents available
Recruitment status
Study complete
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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