Supersaturation and Precipitation of Diclofenac in the Stomach of Healthy Volunteers
Information source: Katholieke Universiteit Leuven
ClinicalTrials.gov processed this data on August 23, 2015 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Supersaturation and Precipitation in the Stomach
Intervention: Diclofenac potassium 50 mg (Drug)
Phase: N/A
Status: Not yet recruiting
Sponsored by: Katholieke Universiteit Leuven
Summary
Investigate the supersaturation and precipitation behaviour of diclofenac in the stomach of
healthy volunteers.
Clinical Details
Official title: Supersaturation and Precipitation of Diclofenac in the Stomach of Healthy Volunteers
Study design: Allocation: Randomized, Endpoint Classification: Pharmacokinetics Study, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Basic Science
Primary outcome: Area under the Concentration - Time Curve
Eligibility
Minimum age: 20 Years.
Maximum age: 35 Years.
Gender(s): Both.
Criteria:
Inclusion Criteria:
- Healthy volunteers
- Age 20 - 35 years
Exclusion Criteria:
- Illness
- Acute / Chronic gastric disorder
- Use of medicine
- (possible) pregnancy
- Frequent exposure to X-rays during the past year
- HIV / Hepatitis B Virus or Hepatitis C Virus infection
Locations and Contacts
Additional Information
Starting date: December 2013
Last updated: December 10, 2013
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