Skip to main content
OpenTrials
Completed

NCT Number: NCT02007577

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, 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.

Completed

Looking for future studies?

Notify Me

Key information

Age range

30 year–60 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Stanford University School of Medicine

Stanford, California, 94305, United States

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Healthy volunteers,
  • BMI 25-35kg/m2,
  • Without severe anemia, kidney, liver disease or any current GI ulcers or bleeding
  • Or on any medication contraindicated with salsalate

Exclusion criteria

  • Recent history of GI bleed or ulcers,
  • CVD or on anticoagulants
  • Severe kidney or liver disease
  • Allergies to aspirin
  • Taking aspirin or anti inflammatory medication on a regular basis and cannot be taken off for the duration of the study

Treatment and study plan

Salsalate

Drug

Participants will take 3, 500 mg tablets with breakfast and 4, 500 mg tablets with dinner

Placebo

Drug

Participants will take 3 tablets with breakfast and 4 tablets with dinner

Primary outcomes

  1. Quantification of Insulin Action With the Insulin Suppression Test (IST)

    Time frame: after treatment for one month

    Compare changes in insulin sensitivity as assesses by the IST before and after treatment between salsalate and placebo group

Secondary outcomes

  1. Quantification of Insulin Clearance With the Graded Glucose Infusion Test (GGIT)

    Time frame: one month on treatment

    compare changes in insulin clearance as assessed by the GGIT before and after treatment with salsalate to placebo

Sponsors and collaborators

Lead sponsor

Stanford University

Other

Registry information

Important dates

Study start
2010
Primary completion
2013
Study completion
2013
First posted
Dec 11, 2013
Registry last updated
May 5, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.