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ABOUT THIS STUDY
taste of formulation
Study Location
FOR MORE INFORMATION
Contact a representative by phone, email, or visiting the study website. Please see the references below:
By phone
Pfizer Clinical Trials Contact Center
1-800-718-1021
Eligibility Criteria
condition
None Volunteer
Sex
Females and Males
Age
18-75 years
Inclusion Criteria
Show details
- Healthy
Exclusion Criteria
Show details
- History of hypersensitivity to test compounds or excipients.
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None VolunteerTaste Test of a New Formulation of Sildenafil (Revatio)
NCT00768573
- Cambridge, Massachusetts
ALL GENDERS
18 Years+
years
MULTIPLE SITES
Advanced Information
Descriptive Information | ||||
---|---|---|---|---|
Brief Title | Taste Test of a New Formulation of Sildenafil (Revatio) | |||
Official Title | A Single-Blind Study In Healthy Adult Volunteers To Investigate The Palatability Of Different Oral Suspension Formulations Of Revatio® | |||
Brief Summary | taste of formulation | |||
Detailed Description | taste test None | |||
Study Type | Observational | |||
Study Design | Time Perspective: Prospective | |||
Target Follow-Up Duration | Not Provided | |||
Biospecimen | Not Provided | |||
Sampling Method | Probability Sample | |||
Study Population | Healthy volunteers | |||
Condition | None Volunteer | |||
Intervention | Drug: sildenafil
Oral suspension of sildenafil. | |||
Study Groups/Cohorts | 1. Taste test
Intervention: Drug: sildenafil | |||
Publications * | Not Provided | |||
* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline. | ||||
Recruitment Information | ||||
Recruitment Status | Completed | |||
Actual Enrollment | 4 | |||
Original Actual Enrollment | 8 | |||
Actual Study Completion Date | January 2008 | |||
Actual Primary Completion Date | January 2008 (Final data collection date for primary outcome measure) | |||
Eligibility Criteria | Inclusion Criteria:
Exclusion Criteria:
| |||
Sex/Gender |
| |||
Ages | 18 Years to 75 Years (Adult, Older Adult) | |||
Accepts Healthy Volunteers | Yes | |||
Contacts | Contact information is only displayed when the study is recruiting subjects | |||
Listed Location Countries | United States | |||
Removed Location Countries | ||||
Administrative Information | ||||
NCT Number | NCT00768573 | |||
Other Study ID Numbers | A1481257 | |||
Has Data Monitoring Committee | No | |||
U.S. FDA-regulated Product | Not Provided | |||
IPD Sharing Statement | Not Provided | |||
Responsible Party | Pfizer | |||
Study Sponsor | Pfizer | |||
Collaborators | Not Provided | |||
Investigators |
| |||
PRS Account | Pfizer | |||
Verification Date | April 2015 |