Effect of Proton Pump Inhibitors on Endothelial Function

Phase 1

Completed

• Conditions: Endothelial Dysfunction
• Interventions: Drug: Placebo; Drug: Lansoprazole

• Registration Number: NCT02022280
• Lead Sponsor: Stanford University

Brief Summary

In this randomized controlled crossover study, the investigators propose to test the hypothesis that proton pump inhibitors (PPIs) increase plasma levels of asymmetric dimethylarginine (ADMA), which is a marker of endothelial dysfunction. The authors propose to evaluate ADMA concentrations and vascular function analysis in healthy volunteers and adults with a history of cardiovascular disease given PPI vs placebo for four weeks each.

Detailed Description

Not available

Study Timeline

• Study Start: 2013-03
• Study First Submitted: 2013-12-03
• Study First Submitted QC: 2013-12-20
• Study First Posted: 2013-12-27
• Primary Completion: 2014-05
• Study Completion: 2014-05
• Status Verified: 2022-08
• Last Update Submitted: 2022-08-19
• Last Update Posted: 2022-08-23

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 21

Inclusion Criteria

• Healthy male or female volunteers aged 18 to 75 years (n=10) or male or female volunteers with a history of coronary or peripheral artery disease (n=10)
• Able to understand the nature of the study and to give written informed consent
• Able to communicate well with the investigator himself or his/her representatives
• Body Mass Index between 18 kg/m^2 and 35 kg/m^2 at the screening visit
• Creatinine <1.5, and liver enzymes <2x normal, with all laboratory tests considered normal or of no significant clinical relevance to the study by the investigator

Exclusion Criteria

• Contra-indication to proton pump inhibitor treatment
• Current treatment with PPI or H2 antagonist, and not able to tolerate withdrawal or washout of medication.
• Current or historical evidence of clinically severe cardiovascular, neurological, hematological, hepatic, gastrointestinal, renal, pulmonary, endocrinological, metabolic or psychiatric disease.
• Any other acute or chronic disease which could influence the volunteer's health and/or the study results
• Presence or history of malabsorption or any gastrointestinal surgery except appendectomy or hernia repair
• Use of enzyme inducers or enzyme inhibitor drugs within the last three months before the first drug administration
• Participation in another ongoing clinical trial
• Past or current drug exposure amounting to drug abuse or addiction
• Past or current alcohol exposure amounting to alcohol abuse or addiction (i.e. > 28 units per week for males, where 1 unit = one measure of spirit (25 mL), one glass of wine (125 mL) or 1/2 pint beer)
• Donation of blood or any other major blood loss (>500 mL) within three months before the study
• Unwilling or unable to comply with the study protocol for any reason or in the opinion of the investigator should not participate in the study
• Positive test for hepatitis B surface antigen, hepatitis C antibody, HIV-1 or HIV-2 antibody at screening
• Known allergy or intolerance to any other compound in the study drug or any other closely related compound

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: CROSSOVER

Arm && Interventions

Group	Intervention	Description
Vitamin pill	Placebo	-
Proton Pump Inhibitor	Lansoprazole	Lansoprazole (Prevacid)

Primary Outcome Measures

Name	Time	Method
Change in reactive hyperemia index as measured by peripheral arterial tonometry (EndoPAT)	Baseline, 1 week, 5 weeks, 7 weeks, 11 weeks, 12 weeks

Secondary Outcome Measures

Name	Time	Method
Change in blood ADMA level	Baseline, 1 week, 5 weeks, 7 weeks, 11 weeks, 12 weeks

Trial Locations

Locations (1)

Stanford University; 🇺🇸 Stanford, California, United States