Effect of Chronic ACE and DPP4 Inhibition on Blood Pressure

NACompletedINTERVENTIONAL
Enrollment

106

Participants

Timeline

Start Date

June 30, 2014

Primary Completion Date

May 31, 2020

Study Completion Date

August 31, 2020

Conditions
Type 2 Diabetes MellitusHypertension
Interventions
DRUG

Placebo

"Subjects will receive two capsules of placebo to preserve the blinding of the study.~In a separate period, subjects will receive one capsule of placebo and one capsule of sitagliptin."

DRUG

Sitagliptin

Subjects will receive sitagliptin 100mg daily for 7 days. In addition, subjects will receive either aprepitant or a capsule of placebo to preserve the blinding of the study.

DRUG

Aprepitant

Subjects will receive aprepitant (125 mg on the first day followed by 80mg/d) for 7 days along with sitagliptin.

OTHER

Mixed Meal Test (MMT)

The first 18 subjects per arm/ group will undergo a mixed meal test on the 7th day of each medication intervention. This will take place after the first half of the study day at the clinical research center, following a 30 minute rest. Subjects will ingest a shake (combination of fixed carbohydrates/ fat/ protein) and have blood pressure, heart rate, and venous blood sample measurements collected for 4 hours after the meal.

Trial Locations (1)

37232

Vanderbilt University, Nashville

All Listed Sponsors
lead

Vanderbilt University

OTHER

NCT02130687 - Effect of Chronic ACE and DPP4 Inhibition on Blood Pressure | Biotech Hunter | Biotech Hunter