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OpenTrials
Completed

NCT Number: NCT00926926

Effects of Oxybutynin Topical Gel on Gastric Emptying

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

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Key information

Conditions

Age range

18 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Phase 1

Primary location

Saint Charles, Missouri, United States

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Oxybutynin Chloride Gel

Drug

Once daily for 7 days, followed by single dose of acetaminophen

Placebo Gel

Drug

Once daily for 7 days, followed by single dose of acetaminophen

Primary outcomes

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

    Time frame: After 7 days of treatment

Sponsors and collaborators

Lead sponsor

Watson Pharmaceuticals

Industry

Registry information

Official study title

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

Important dates

Study start
2009
Primary completion
2009
Study completion
2009
First posted
Jun 24, 2009
Registry last updated
Oct 8, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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