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Effects of Oxybutynin Topical Gel on Gastric Emptying

Information source: Watson Pharmaceuticals
ClinicalTrials.gov processed this data on August 23, 2015
Link to the current ClinicalTrials.gov record.

Condition(s) targeted: Healthy

Intervention: Oxybutynin Chloride Gel (Drug); Placebo Gel (Drug)

Phase: Phase 1

Status: Completed

Sponsored by: Watson Pharmaceuticals

Official(s) and/or principal investigator(s):
Scott Olsen, MPH, Study Director, Affiliation: Watson Laboratories


This study explores the effect of oxybutynin topical gel on gastric emptying

Clinical Details

Official title: Effect of Oxybutynin Chloride Topical Gel on Gastric Emptying, Using the Acetaminophen Absorption Test

Study design: Allocation: Randomized, Endpoint Classification: Pharmacokinetics Study, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Basic Science

Primary outcome: The effect of oxybutynin chloride topical gel administration on gastric emptying will be assessed by comparing the single dose relative bioavailability of acetaminophen


Minimum age: 18 Years. Maximum age: N/A. Gender(s): Female.


Inclusion Criteria:

- Adult, healthy, post-menopausal females

Exclusion Criteria:

- Patients for whom OTG or acetaminophen is contraindicated.

- Abnormality of the GI tract.

- Taking drugs that affect gastric motility.

Locations and Contacts

St. Charles, Missouri, United States
Additional Information

Starting date: June 2009
Last updated: October 5, 2012

Page last updated: August 23, 2015

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