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NCT02007577 · ClinicalTrials.gov registry record · NA

Beneficial Effect of Salicylates: Insulin Action, Secretion or Clearance?

A NA study of Pre Diabetes and Insulin Resistant, sponsored by Stanford University.

Completed
Registry status
NA
Development phase
41
Enrollment target
1
Study location

NCT02007577 is a NA study of Pre Diabetes and Insulin Resistant that has completed, run by Stanford University. The registered enrollment target is 41 participants, below the 729-participant average among 59 other Pre Diabetes trials with a reported enrollment target (94% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT02007577, a NA study of Pre Diabetes and Insulin Resistant, has completed, sponsored by Stanford University.

COMPLETED
Registry status
NA
Development phase
41 participants
Enrollment target
1
Study location

Study Summary

The possibility that obesity-associated inflammatory changes may play a role in the pathogenesis of type 2 diabetes (2DM) has led to increased interest in the possibility that salicylates might represent a useful treatment to improve glucose tolerance. Several studies, performed in patients with 2DM, as well as in nondiabetic, obese individuals, have demonstrated that salicylates have beneficial effects on glucose and insulin metabolism, but have not led to a coherent view as to the mechanism(s) involved. In this research proposal we will use specific methods to quantify insulin mediated glucose uptake (IMGU), glucose-stimulated insulin secretion rate (GS-ISR), and insulin clearance (I-Cl) in overweight/obese, nondiabetic, insulin resistant individuals. We will use the insulin suppression test (IST) to quantify IMGU in nondiabetic, overweight/obese volunteers to identify those individuals who are sufficiently insulin resistant to be enrolled in this study. We will then use the graded glucose infusion technique in these insulin resistant subjects to generate specific measures of both GS-IS and I-Cl. Following these baseline measurements, salsalate or placebo will be administered for one month to the participants, after which time the IST and the graded glucose infusion will be repeated to quantify and compare the changes in IMGU, GS-ISR, and I-Cl that have resulted from salsalate versus placebo. These results will provide for the first time quantitative data of the effect of salicylates on IMGU, GS-ISR, and I-Cl in overweight/obese, insulin resistant, nondiabetic individuals.

Interventions

  • DRUG Placebo
  • DRUG salsalate

Study Locations (1)

California

  • Stanford University School of Medicine - Stanford

Trial Details

FieldValue
Enrollment Target 41 participants
Start Date 2010-07
Est. Completion 2013-11
Phase NA

Sponsor

Stanford University

1,744 total trials

What the Registry Record Tells You About NCT02007577

The ClinicalTrials.gov registry entry for NCT02007577 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 41 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 729-participant average among 59 other Pre Diabetes trials with a reported enrollment target (94% lower). The listed sponsor is Stanford University, which has 1,744 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Pre Diabetes appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.

NCT02007577 reports 1 study location spanning 1 distinct geographic area - top geographies include California.

Frequently Asked Questions

What is clinical trial NCT02007577 about?

NCT02007577 is a clinical study titled "Beneficial Effect of Salicylates: Insulin Action, Secretion or Clearance?". The possibility that obesity-associated inflammatory changes may play a role in the pathogenesis of type 2 diabetes (2DM) has led to increased interest in the possibility that salicylates might represent a useful treatment to improve glucose tolerance. Several studies, performed in patients with 2DM...

What is the current status of trial NCT02007577?

This trial is currently completed. It is a NA study. The enrollment target is 41 participants. The study started on 2010-07. Estimated completion is 2013-11.

What conditions does trial NCT02007577 study?

This clinical trial studies the following conditions: Pre Diabetes, Insulin Resistant.

What interventions are being tested in trial NCT02007577?

The interventions under investigation include: Placebo (DRUG), salsalate (DRUG).

Who is sponsoring clinical trial NCT02007577?

This trial is sponsored by Stanford University, which has 1,744 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02007577 being conducted?

This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.