CuraLin Herbal Supplement for Type 2 Diabetes

NCT05267925 | Terminated

• 1 other identifier: RBKK8321
• Study Type: interventional
• Target: 1
• Locations: 1 country
• Sites: 2

Brief Summary

The purpose of this study is to provide preliminary data necessary for a larger, controlled trial of CuraLin as a treatment option for T2DM. This study will also fill the gap in literature surrounding herbal medicine in the treatment of T2DM. The use of herbal preparations for diabetes has increased globally, and given the costs, adverse effects, lack of clinical outcome improvement, and minimal A1c reductions associated with medications, safer, more affordable alternatives need to be explored. CuraLin™ is a dietary supplement manufactured by NutraStar Inc. and sold by CuraLife; it is a blend of nine ayurvedic plants and herbs taken three times daily, after meals for the management of diabetes. It is hypothesized that CuraLin will be safely tolerated among adults with Type 2 Diabetes Mellitus, and will improve glucose control and cardiometabolic risk factors over this 12 week study.

Conditions

Type 2 Diabetes

Outcome Measures

Primary Outcomes (5)

• Hemoglobin A1C

  Hemoglobin is the oxygen-carrying component of red blood cells. In the presence of sustained elevated glucose levels, glucose non-enzymatically binds to hemoglobin, leading to the formation of glycated hemoglobin, and later, advanced glycation end products (AGEs). AGEs are responsible for many of the complications of T2DM. Thus, HbA1c, in conjunction with fasting blood glucose, is used as diagnostic criteria for T2DM (HbA1c ≥ 6.5%), and is used as a marker of glycemic control in diabetic individuals. As the life cycle of a red blood cell is approximately 90 days, serum HbA1c measurements are a snapshot of the percent of glycated hemoglobin over the prior two to three months, and thus serve as a snapshot of glycemic control in T2DM. HbA1c will be expressed as a percentage.

  12 Weeks

• Gamma-glutamyltransferase (GGT)

  Concentration of the enzyme Gamma-glutamyltransferase (GGT) in the blood is considered a measure of liver inflammation and oxidative stress. Liver function markers will be expressed as IU/L.

  12 Weeks

• Aspartate aminotransferase (AST)

  Concentration of the enzyme aspartate aminotransferase (AST) in the blood is considered a measure of liver inflammation. Liver function markers will be expressed as IU/L.

  12 Weeks

• Alanine aminotransferase (ALT)

  Concentration of the enzyme alanine aminotransferase (ALT) in the blood is considered a measure of liver inflammation. Liver function markers will be expressed as IU/L.

  12 Weeks

• Homeostatic Model Assessment of Insulin Resistance

  The Homeostatic model assessment (HOMA) of β- cell function and insulin resistance (IR) is a calculated ratio of fasting plasma insulin to glucose, and reflects the balance between hepatic glucose output and β- cell insulin secretion. It has been used in greater than 500 research publications to provide an estimate of insulin sensitivity and β- cell function, and is used to predict the level of insulin resistance. In patients with T2DM, the HOMA-IR is able to assess changes in β-cell function and IR, and thus, provide a reflection of treatment effects. The HOMA-IR will be expressed as a number, where '1' is considered normal, and anything above '1' is reflective of some degree of insulin resistance.

  12 Weeks

Secondary Outcomes (7)

• Fasting Blood Glucose

  12 Weeks

• Estimated glomerular filtration rate

  12 Weeks

• Triglycerides

  12 Weeks

• LDL:HDL ratio

  12 Weeks

• BMI

  12 Weeks

Other Outcomes (1)

• PROMIS-29 Health-related Quality of Life

  12 Weeks

Study Arms (1)

Intervention

EXPERIMENTAL

All participants will be asked to take the dietary herbal supplement CuraLin for the duration of the study. All participants will take 2 capsules orally, three times per day following meals for 12 weeks.

Dietary Supplement: CuraLin

Interventions

CuraLin DIETARY_SUPPLEMENT

CuraLin™ is a dietary supplement manufactured by NutraStar Inc. and sold by CuraLife; it is a blend of nine ayurvedic plants and herbs. The CuraLin formulation contains the following ingredients (per 2 capsules): * Mormordica charantia (fruit) - 300mg * Gymnema sylvestre (leaf) - 80mg * Trigonella foenum-Graecum (seed) - 100mg * Curcuma longa (rhizome) - 100mg * Phyllanthus embilica officinalis (fruit) - 100mg * Swertia chiraytia (leaf) - 80mg * Syzgium Cumini (seed) - 100mg * Neopicrorhiza Picrorhiza/Scrophulariiflora Kurroa (root) - 100mg * Cinnamoum verum/zeylanicum - 40 mg * Hydroxypropyl methylcellulose * Rice Flour

Intervention

Eligibility Criteria

• Age: 18 Years - 75 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Community-dwelling adults ≥18 and ≤ 75 years of age.
• Have an existing diagnosis of type 2 diabetes without known complications; i.e. eye damage (retinopathy), nerve damage (diabetic peripheral neuropathy), kidney damage (diabetic kidney disease), or heart damage (recent myocardial infarction or severe congestive heart failure).
• Must be on a stable dose (i.e. consistent dose for three months or greater) of all medications.
• Must be on a stable dose of dietary supplements for one month prior to enrollment.
• Have a serum hemoglobin A1c between 7% and 9.5%.
• Able to communicate via email, fill out a computer-administered questionnaire, and to read and write in English.
• Willing to have blood drawn at 3 separate time points.
• Willing to take an herbal supplement three times a day, daily, for 12 weeks.
• Willing to abstain from new anti-diabetic therapies, vitamins, minerals, dietary supplements, and lipid-lowering agents for 12 weeks.
• Willing and able to follow the study protocol and attend study visits.
• Approved to be eligible for study participation at the discretion of the Principal Investigators, after review of the Formal Eligibility Screen results.

You may not qualify if:

• Allergy to any ingredient found in the study product (Mormordica charantia (fruit), Gymnema sylvestre (leaf), Trigonella foenum-Graecum (seed), Curcuma longa (rhizome), Phyllanthus embilica officinalis (fruit), Swertia chiraytia (leaf), Syzgium Cumini (seed), Neopicrorhiza Picrorhiza/Scrophulariiflora Kurroa (root), Cinnamoum verum/zeylanicum, Hydroxypropyl methylcellulose, Rice Flour).
• Current use of insulin.
• Current use of CuraLin or any dietary supplement that has the same ingredients as CuraLin (see list of ingredients above).
• Current use of the following lipid-lowering medications: Ezetimibe (Zetia), Cholestyramine (Prevalite, Questran, Questran Light), Colesevelam (Welchol), or Colestipol (Colestid, Colestid Flavored).
• History of myocardial infarction or stroke within the last 6 months, current coronary artery disease, unstable angina, uncontrolled hypertension (i.e. systolic \> 180 or diastolic \> 110), congestive heart failure, or stated history of coronary bypass surgery or heart stent placement.
• Current active diabetic ulcers or history of diabetic neuropathy.
• Active malignancy, with the exception of basal cell carcinoma, squamous cell carcinoma, and/or carcinoma in situ of the cervix.
• Current diagnosis of Small Intestinal Bacterial Overgrowth (SIBO), Small Intestinal Fungal Overgrowth (SIFO), Inflammatory Bowel Disease (IBD; i.e. Crohn's or Ulcerative Colitis), or other diagnosed pathology of the gastrointestinal tract (excluding Irritable Bowel Syndrome, \[IBS\]).
• Presence of an unstable and/or significant medical disorder that would compromise the participant's safety to take part in the study.
• Planned elective surgery within the next 12 weeks.
• Pregnant, nursing, or planning a pregnancy within the next 12 weeks.
• Women of childbearing age not using standard birth control measures.
• History of liver and/or kidney disease.

Sponsors & Collaborators

• National University of Natural Medicine: lead

Study Sites (2)

National University of Natural Medicine

Portland, Oregon, 97201, United States

Location

Institute of Complementary Medicine

Seattle, Washington, 98122, United States

Location

MeSH Terms

Conditions

Diabetes Mellitus, Type 2

Condition Hierarchy (Ancestors)

Diabetes Mellitus; Glucose Metabolism Disorders; Metabolic Diseases; Nutritional and Metabolic Diseases; Endocrine System Diseases

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: NA
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: January 3, 2022
• First Posted: March 7, 2022
• Study Start: January 8, 2022
• Primary Completion: April 14, 2022
• Study Completion: April 14, 2022
• Last Updated: April 5, 2023

Record last verified: 2023-04

Data Sharing

• IPD Sharing: Will not share

Locations

US (2)