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Supersaturation and Precipitation in the Stomach | Supersaturation and Precipitation of Diclofenac in the Stomach of Healthy Volunteers

Supersaturation and Precipitation in the Stomach research study

What is the primary objective of this study?

Investigate the supersaturation and precipitation behaviour of diclofenac in the stomach of healthy volunteers.

Who is eligible to participate?

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

Which medical condition, disease, disorder, syndrome, illness, or injury is researched?

Supersaturation and Precipitation in the Stomach

Study Interventions

Interventions can include giving participants drugs, medical devices, procedures, vaccines, and other products that are either investigational or already available or noninvasive approaches such as surveys, education, and interviews.

Drug:Diclofenac potassium 50 mgDiclofenac potassium 50 mg

Study Arms

Research studies and clinical trials typically have two or more research arms. An arm is a group of people who receive the same treatment in the study.

Nutritional StateFed vs. Fasted State Diclofenac potassium 50 mg

Use of a PPINexiam (esomeprazole) 40 mg Diclofenac potassium 50 mg

Study Status

Unknown status

Start Date: December 2013

Completed Date: December 2014

Phase: N/A

Type: Interventional

Design:

Primary Outcome: Area under the Concentration - Time Curve

Secondary Outcome:

Study sponsors, principal investigator, and references

Principal Investigator:

Lead Sponsor: Katholieke Universiteit Leuven

Collaborator:

More information:https://clinicaltrials.gov/show/NCT02007161

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