N/A
N=41
Beneficial Effect of Salicylates: Insulin Action, Secretion or Clearance?
Pre Diabetes · Insulin Resistant
Bottom Line
View on ClinicalTrials.gov: NCT02007577 ↗Enrolled (actual)
41
Serious AEs
0.0%
Results posted
May 2016
Primary outcome: Primary: Quantification of Insulin Action With the Insulin Suppression Test (IST) — -3; 2 mmol/L
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- salsalate (Drug); Placebo (Drug)
- Age
- Adult · 30+ yrs
- Sex
- All
- Sponsor
- Stanford University
- Primary completion
- Nov 2013
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Quantification of Insulin Action With the Insulin Suppression Test (IST) |
-3; 2 | — |
| SECONDARY Quantification of Insulin Clearance With the Graded Glucose Infusion Test (GGIT) |
-6; 0 | — |
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.
Eligibility Criteria
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
Data sourced from ClinicalTrials.gov (NCT02007577). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.