search
Back to results

Effects of Capros in Patients With Type-1 Diabetes (CarposT1D)

Primary Purpose

Type I Diabetes

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Capros
Sponsored by
Ohio State University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Type I Diabetes focused on measuring Hyperglycemia, Capros, Type 1 Diabetes

Eligibility Criteria

10 Years - 60 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Subjects must be 10 - 60 yrs. of age
  • Type 1 Diabetes using Continuous Glucose Monitoring (CGM) for at least the last 3 months
  • Less than 10% variation in prescribed long acting dosages in the previous 3 months

Exclusion Criteria:

  • Individuals who are deemed unable to understand the procedures, risks and benefits of the study, i.e. informed consent will be excluded from the study
  • Females who are pregnant
  • Individuals who are therapeutically immuno-compromised
  • Prisoners
  • Anyone with a known allergy to amla fruit
  • Current use of any of the following medications will result in exclusion:
  • Steroids (Prednisone, etc.)
  • Immunosuppressants
  • Accutane (last 6 months)

Sites / Locations

  • Carepoint East 543 Taylor Ave.
  • Martha Morehouse Medical Plaza 2050 Kenny Road
  • Davis Heart and Lung Research Institute

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Type 1 Diabetics using CGM

Arm Description

Type 1 diabetics using Continuous Glucose MonitoringCGM to take 500 mg daily of Capros supplement (250 mg twice a day) at lunch and dinner.

Outcomes

Primary Outcome Measures

Effect of Capros on Blood Glycemic Index
To determine the effect on blood glycemic index in Type 1 Diabetics with taking the nutritional supplement Capros

Secondary Outcome Measures

Full Information

First Posted
June 26, 2015
Last Updated
November 18, 2019
Sponsor
Ohio State University
Collaborators
Natreon, Inc.
search

1. Study Identification

Unique Protocol Identification Number
NCT02634216
Brief Title
Effects of Capros in Patients With Type-1 Diabetes
Acronym
CarposT1D
Official Title
Effects of Capros Supplementation on Hyperglycemia in Patients With Type-1 Diabetes
Study Type
Interventional

2. Study Status

Record Verification Date
November 2019
Overall Recruitment Status
Completed
Study Start Date
January 2015 (undefined)
Primary Completion Date
May 25, 2016 (Actual)
Study Completion Date
May 25, 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Ohio State University
Collaborators
Natreon, Inc.

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this 12 week longitudinal study is to test the effect of the dietary supplement, Capros, on blood glycemic index of Type 1 diabetics that have a sensor that provides continuous glucose monitoring (CGM). 20 Type 1 Diabetics will take the Capros supplement for 12 weeks to determine the effect of blood glycemic index. Capros, is a generally safe dietary supplement currently sold over the counter in the United States. Type 1 diabetes also known as juvenile diabetes is commonly diagnosed in children and young adults. Insulin is converted into energy needed for daily living, and with diabetes, insulin is not produced in the body as it should causing many problems. In traditional Indian medicine, the gooseberry Phyllanthus emblica has been used for thousands of years as an effective source of polyphenols and antioxidants. A 12 week longitudinal study to determine the effect of the dietary supplement, Capros, on the blood glycemic index in patients with Type 1 diabetes (T1D).
Detailed Description
There are a total of 4 study visits,over the course of 12 weeks. These visits will occur on weeks 1, 4, 8, and 12. At each study visit the the following will be recorded: Age, Sex, Pulse, height, weight, CGM real time measurement and the following non-medical information will be recorded: Address, Phone number and Email address ( will be recorded at the first visit and will be asked if anything has changed at the reoccurring visits). The following will happen at each visit: Visit 1 (Week 0): The subject will be presented with informed consent. Data will be collected on a data collection sheet, a finger stick for A1C will be obtained (if not completed as SoC), Continuous Glucose Monitoring will be downloaded, UPT for WCBP will be performed, the subject will be given a 4-week supply of the Capros supplement and a subject diary. The subject will be given a subject diary to document their morning/evening sugar and the time of when participants take the supplements. The subject will be asked to bring in the diary to each follow-up visit to check for compliance verification. Visit 2 and 3 (Week 4 and 8): The following activities will take place during these visits: AE review, concomitant medications review, weight, vital signs, CGM download, pill count and distribution, collect previous diary and provide new. Visit 4 (Week 12): The following activities will take place during these visits: AE review, concomitant medications review, weight, vital signs, CGM download, pill count, collect previous diary. Also, at this visit, a finger stick for A1C (if not completed as SoC), no further distribution of supplements. Taking the supplement: After receiving the supplement, the subject is instructed to take 2 capsules per day by mouth, once with food around lunchtime and once with food around dinner time for a total of 12 weeks. The subjects will be asked to keep all empty bottles/ any remaining Capros supplements and bring them to each follow-up visit for a compliance check. Participants will receive a new 4-week supply of supplements at study visits 2 and 3. Risks for participating in this study are extremely low. Capros is a dietary supplement derived from the Indian Gooseberry, and contains no artificial ingredients, is non-toxic and is safely tolerated among humans. Capros is currently sold over the counter in the U.S. and has no known side effects; however an allergic reaction to the supplement is possible. There is a potential risk for hypoglycemia while taking this supplement. In the even that this occurs, subjects are instructed to follow their primary care physician instructions for this and record it on their data log. This is not a treatment study so subjects may have no direct benefit while taking the supplement. The investigators are looking to monitor and observe if any changes take place with participants blood sugar level over the course of the study.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Type I Diabetes
Keywords
Hyperglycemia, Capros, Type 1 Diabetes

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
24 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Type 1 Diabetics using CGM
Arm Type
Experimental
Arm Description
Type 1 diabetics using Continuous Glucose MonitoringCGM to take 500 mg daily of Capros supplement (250 mg twice a day) at lunch and dinner.
Intervention Type
Dietary Supplement
Intervention Name(s)
Capros
Intervention Description
250 mg BID
Primary Outcome Measure Information:
Title
Effect of Capros on Blood Glycemic Index
Description
To determine the effect on blood glycemic index in Type 1 Diabetics with taking the nutritional supplement Capros
Time Frame
12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
10 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Subjects must be 10 - 60 yrs. of age Type 1 Diabetes using Continuous Glucose Monitoring (CGM) for at least the last 3 months Less than 10% variation in prescribed long acting dosages in the previous 3 months Exclusion Criteria: Individuals who are deemed unable to understand the procedures, risks and benefits of the study, i.e. informed consent will be excluded from the study Females who are pregnant Individuals who are therapeutically immuno-compromised Prisoners Anyone with a known allergy to amla fruit Current use of any of the following medications will result in exclusion: Steroids (Prednisone, etc.) Immunosuppressants Accutane (last 6 months)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Gayle M. Gordillo, M.D.
Organizational Affiliation
Ohio State University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Carepoint East 543 Taylor Ave.
City
Columbus
State/Province
Ohio
ZIP/Postal Code
43203
Country
United States
Facility Name
Martha Morehouse Medical Plaza 2050 Kenny Road
City
Columbus
State/Province
Ohio
ZIP/Postal Code
43210
Country
United States
Facility Name
Davis Heart and Lung Research Institute
City
Columbus
State/Province
Ohio
ZIP/Postal Code
43212
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
22701284
Citation
Hiraganahalli BD, Chinampudur VC, Dethe S, Mundkinajeddu D, Pandre MK, Balachandran J, Agarwal A. Hepatoprotective and antioxidant activity of standardized herbal extracts. Pharmacogn Mag. 2012 Apr;8(30):116-23. doi: 10.4103/0973-1296.96553.
Results Reference
result
PubMed Identifier
12065146
Citation
Sabu MC, Kuttan R. Anti-diabetic activity of medicinal plants and its relationship with their antioxidant property. J Ethnopharmacol. 2002 Jul;81(2):155-60. doi: 10.1016/s0378-8741(02)00034-x.
Results Reference
result

Learn more about this trial

Effects of Capros in Patients With Type-1 Diabetes

We'll reach out to this number within 24 hrs