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Clinical Trials/NCT03011645
NCT03011645
Terminated
Phase 1

Gene-by-Stress Interactions in Intervention Studies Significance

Duke University1 site in 1 country7 target enrollmentMay 24, 2018

Overview

Phase
Phase 1
Intervention
Ziprasidone
Conditions
Cardiovascular Diseases
Sponsor
Duke University
Enrollment
7
Locations
1
Primary Endpoint
Change in peak blood cortisol during the metabolic stress of an OGTT
Status
Terminated
Last Updated
6 years ago

Overview

Brief Summary

The purpose of this study is to identify gene variants that increase risk of cardiovascular disease (CVD) and type 2 diabetes, particularly genes related to stress factors.

Detailed Description

In Aim 3, 100 subjects who participated in previous studies will be recruited to test the ability of a 5HTR2C agonist (lorcaserin) to increase and antagonist (ziprasidone) to reduce cortisol response to mental and metabolic stress in men carrying the rs6318 C allele and women in the rs6318 CC genotype of 5HTR2C. Lorcaserin is serotonin receptor agonist indicated for use as a weight loss drug. Ziprasidone is an antipsychotic indicated for treatment of bipolar disorder. Subjects will be treated with a single dose of each drug, 1 to 2 weeks apart, followed by a mental stress test and an oral glucose tolerance test with multiple blood draws. Each subject will also receive a placebo drug during one of the study visits.

Registry
clinicaltrials.gov
Start Date
May 24, 2018
End Date
January 28, 2020
Last Updated
6 years ago
Study Type
Interventional
Study Design
Factorial
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Men and women who have been enrolled in the STRRIDE, ENHANCED, and/or REMIT studies age 18 years or greater.
  • Ability and willingness to provide informed consent.
  • Individuals with specific genotypes as determined from our previous work on their samples through Aim 1 of this project.

Exclusion Criteria

  • Women who are known to be pregnant, intend to become pregnant, or breast-feeding will be excluded. Women who are of child bearing potential (under age 55) will be informed that they will need to have their urine tested for pregnancy and that they should not participate in the research if they are not willing to have the Investigators provide them with information on positive pregnancy test results. Subjects will be informed that the pregnancy testing is not being performed for clinical purposes and that the testing is not a substitute for their regular medical care if they need to know whether or not they may be pregnant.
  • History of Type II diabetes mellitus.
  • History of prolonged QT interval.
  • Participation in an investigational drug trial within the last 30 days.
  • Already taking either ziprasidone or lorcaserin or any potential confounding medications, for example, other weight loss medications or psychotropic medications.
  • Unwillingness to fast for at least 6 hours prior to the research study visit.

Arms & Interventions

Ziprasidone

Ziprasidone 60 mg tablet by mouth, once a day for one day.

Intervention: Ziprasidone

Lorcaserin

Lorcaserin 20 mg tablet by mouth, once a day for one day.

Intervention: Lorcaserin

Placebo Oral Tablet

Sugar pill (in place of ziprasidone and lorcaserin) by mouth, once a day for one day.

Intervention: Placebo Oral Tablet

Outcomes

Primary Outcomes

Change in peak blood cortisol during the metabolic stress of an OGTT

Time Frame: Baseline to 3-hours post OGTT

Change in peak blood cortisol during the metabolic stress of a mental stress test

Time Frame: Baseline to 3-hours post mental stress test

Secondary Outcomes

  • Area-Under-the-Curve Glucose(Baseline to 2-hours post OGTT)
  • Matsuda Insulin Resistance Index(Baseline to 2-hours post OGTT)

Study Sites (1)

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