search
Back to results

Can Resveratrol Improve Insulin Sensitivity and Preserve Beta Cell Function Following Gestational Diabetes?

Primary Purpose

Gestational Diabetes

Status
Unknown status
Phase
Phase 4
Locations
Canada
Study Type
Interventional
Intervention
Resveratrol
Placebo
Sponsored by
University of Manitoba
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Gestational Diabetes focused on measuring resveratrol,, gestational diabetes,, beta cell function, history

Eligibility Criteria

18 Years - 40 Years (Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Adult women (18 years of age or older) 3 months post-partum with a recent history of first diagnosis of gestational diabetes.
  • Willingness to provide informed consent 3 months post-partum.

Exclusion Criteria:

  • Abnormal glucose tolerance or type 2 diabetes recorded at 3 months post-partum.
  • Breastfeeding beyond 9 months post-partum.
  • Intention to consume resveratrol open label.
  • Intention to drink red wine (more than 4 glasses per week) or eat foods high in resveratrol (grapes, grape juice, peanuts, peanut products).
  • Unwillingness to use two approved types of contraception until one year post-partum and unwillingness to undergo pregnancy test at randomization.
  • Twin pregnancy.
  • Consuming medications with a risk of interaction with resveratrol.
  • Liver disease.
  • Unlikely to be able to comply with study follow-up as judged by social (e.g. transient, not permanent residents, etc.) or geographical considerations.

Sites / Locations

  • Manitoba Institute of Child HealthRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Experimental

Arm Label

Placebo

Resveratrol

Arm Description

Corn starch capsules, 1 capsule twice a day for 3 months

Resveratrol capsules, 250 mg twice a day for 3 months

Outcomes

Primary Outcome Measures

Change in beta cell function
Beta cell function will be assessed by calculating the Insulin Secretion Sensitivity Index-2, a ratio of the area under the curve (AUC) for glucose and the AUC for insulin after an oral glucose tolerance test.

Secondary Outcome Measures

recruitment rates
treatment adherence
Change in insulin sensitivity
Insulin sensitivity will be assessed by calculating the homeostasis model of assessment of insulin resistance (HOMA-IR).

Full Information

First Posted
November 13, 2013
Last Updated
May 9, 2014
Sponsor
University of Manitoba
Collaborators
Manitoba Institute of Child Health
search

1. Study Identification

Unique Protocol Identification Number
NCT01997762
Brief Title
Can Resveratrol Improve Insulin Sensitivity and Preserve Beta Cell Function Following Gestational Diabetes?
Official Title
Can Resveratrol Improve Insulin Sensitivity and Preserve Beta Cell Function Following Gestational Diabetes?
Study Type
Interventional

2. Study Status

Record Verification Date
November 2013
Overall Recruitment Status
Unknown status
Study Start Date
May 2014 (undefined)
Primary Completion Date
December 2015 (Anticipated)
Study Completion Date
December 2016 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Manitoba
Collaborators
Manitoba Institute of Child Health

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to determine if resveratrol supplementation preserves beta cell function and insulin sensitivity in post-partum women following a first diagnosis of gestational diabetes. We hypothesize that daily supplementation with resveratrol will preserve beta cell function and insulin sensitivity.
Detailed Description
Our primary aim is to perform a randomized controlled trial of resveratrol for the improvement of insulin sensitivity and the preservation of beta cell function in post-partum women following a first diagnosis of gestational diabetes. Our long-term goal is to test resveratrol for the secondary prevention of gestational diabetes and type 2 diabetes. We have developed six conditions that should be satisfied by the study to justify project expansion. Therefore, we will be testing hypotheses and computing estimates for the following six outcomes: (1) recruitment numbers, (2) adherence to study treatment, (3) adherence to study visits, (4) insulin sensitivity measured at 12 months post-partum, (5) beta cell function measured at 12 months post-partum, and (6) adverse events. The study is a single-site, parallel, double-blind, randomized, placebo-controlled trial. The study population consists of women recruited during pregnancy who had a confirmed first diagnosis of gestational diabetes, who do not have either diabetes or pre-diabetes when re-tested 3 months post-partum, and who have stopped breastfeeding by 9 months post-partum. They study intervention is resveratrol (or identical placebo) twice daily for a total of 12 weeks from 9 months to 12 months post-partum. Our planned sample size is 112 women based on the hypothesis testing and estimation considerations for the six above-mentioned outcomes.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gestational Diabetes
Keywords
resveratrol,, gestational diabetes,, beta cell function, history

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
112 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Corn starch capsules, 1 capsule twice a day for 3 months
Arm Title
Resveratrol
Arm Type
Experimental
Arm Description
Resveratrol capsules, 250 mg twice a day for 3 months
Intervention Type
Dietary Supplement
Intervention Name(s)
Resveratrol
Other Intervention Name(s)
All Natural Resveratrol 98% Super Strength
Intervention Description
gel-coated capsules to be taken twice a day; one with breakfast and dinner
Intervention Type
Dietary Supplement
Intervention Name(s)
Placebo
Other Intervention Name(s)
Corn starch capsules
Primary Outcome Measure Information:
Title
Change in beta cell function
Description
Beta cell function will be assessed by calculating the Insulin Secretion Sensitivity Index-2, a ratio of the area under the curve (AUC) for glucose and the AUC for insulin after an oral glucose tolerance test.
Time Frame
baseline and 3 months after intervention
Secondary Outcome Measure Information:
Title
recruitment rates
Time Frame
recruitment rates will be followed throughout the recruitment phase, which is expected to take 2 years maximum
Title
treatment adherence
Time Frame
3 months after intervention
Title
Change in insulin sensitivity
Description
Insulin sensitivity will be assessed by calculating the homeostasis model of assessment of insulin resistance (HOMA-IR).
Time Frame
baseline and 3 months after intervention
Other Pre-specified Outcome Measures:
Title
change in liver function
Description
liver function will be assessed by measuring plasma concentrations of alanine aminotransferase, aspartate aminotransferase, gamma glutamyltransferase, total bilirubin and conjugated bilirubin.
Time Frame
baseline and 3 months after intervention
Title
change in C-reactive protein
Time Frame
baseline and 3 months after intervention
Title
change in glycated hemoglobin
Time Frame
baseline and 3 months after intervention
Title
change in serum lipids
Time Frame
baseline and 3 months after intervention
Title
change in plasma levels of resveratrol and resveratrol metabolites
Time Frame
baseline and 3 months after intervention

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Adult women (18 years of age or older) 3 months post-partum with a recent history of first diagnosis of gestational diabetes. Willingness to provide informed consent 3 months post-partum. Exclusion Criteria: Abnormal glucose tolerance or type 2 diabetes recorded at 3 months post-partum. Breastfeeding beyond 9 months post-partum. Intention to consume resveratrol open label. Intention to drink red wine (more than 4 glasses per week) or eat foods high in resveratrol (grapes, grape juice, peanuts, peanut products). Unwillingness to use two approved types of contraception until one year post-partum and unwillingness to undergo pregnancy test at randomization. Twin pregnancy. Consuming medications with a risk of interaction with resveratrol. Liver disease. Unlikely to be able to comply with study follow-up as judged by social (e.g. transient, not permanent residents, etc.) or geographical considerations.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Danielle M Stringer, PhD
Phone
(204) 789-3273
Email
dstringer@mich.ca
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Shayne P Taback, MD
Organizational Affiliation
University of Manitoba
Official's Role
Principal Investigator
Facility Information:
Facility Name
Manitoba Institute of Child Health
City
Winnipeg
State/Province
Manitoba
ZIP/Postal Code
R3E 3P4
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Shayne P Taback, MD

12. IPD Sharing Statement

Learn more about this trial

Can Resveratrol Improve Insulin Sensitivity and Preserve Beta Cell Function Following Gestational Diabetes?

We'll reach out to this number within 24 hrs