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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

Page last updated: August 23, 2015

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