Evaluate Retention of an Orally Administered Device Using Gamma Scintigraphy

Completed · Phase 1

Conditions studied: Healthy Subjects

In brief

Single usage, open label study in 16 adult healthy males. Eligible subjects will receive a single usage of the investigational device. Retention of the radiolabeled device will be monitored using gamma scintigraphy.

Key facts

Study ID

NCT00754091

Run by

Procter and Gamble

People needed

16

Starts

2008-06-01

Expected to finish

2008-06-01

Last updated by the study team

2019-03-26

Who can join

Age: 18 and older, up to 40. Sex: male. Healthy volunteers: accepted.

You may qualify if…

• Refrain from nasal, throat, or lung inhalants and exercise for 24 hour prior to the test
• Are able to tolerate the procedure and
• Be generally healthy

You may not qualify if…

• Have history of allergy or hypersensitivity to the study ingredients
• Major diseases
• Taking medication regularly
• Radiation exposure recently

Where it is running

• Walter J Doll, PhD, RPh — Lexington, Kentucky, United States

Full record on ClinicalTrials.gov

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