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Dog-rose, Cranberry Leaves, Cranberry Berries, Alfalfa, Fenugreek, Lemon Beebrush, Urtica and Sumac in Diabetes Mellitus

Primary Purpose

Type 2 Diabetes

Status
Not yet recruiting
Phase
Phase 1
Locations
Iran, Islamic Republic of
Study Type
Interventional
Intervention
Capsules containing the combination products
Placebo capsules
Sponsored by
Tabriz University of Medical Sciences
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Type 2 Diabetes focused on measuring Type 2 diabetes, Insulin resistance, Lipochromin, Vaccinium macrocarpon, Medicago sativa, Trigonella, Fenugreek, Lemon Beebrush, Urtica dioica, Rhus, Sumac

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: At least one year of diagnosis of type 2 diabetes according to the criteria of the World Health Organization, Hemoglobin A1c (HbA1c) > 7.0% or fasting blood glucose > 7.0 mmol/L, Body mass index (BMI) more than 23 kg/m2 and less than 35. Exclusion Criteria: Comorbidities, including type 1 diabetes, cardiovascular disease, thyroid disease, liver disease, kidney disease, cancer, mental disorders, and the use of drugs related to the aforementioned diseases, Pregnancy, Patients with a BMI over 35 who were on a weight loss diet or had taken weight loss supplements for less than 6 months A history of allergy to one of the components of the nestling fruit, carob leaf, carob fruit, alfalfa seed, fenugreek seed, lemon, Nettles and sumac and also Lactating women Regularly consuming cigarettes or alcohol Using psychiatric drugs or insulin Changing in the medication regimen during the trial period. For example, to start receiving insulin therapy, become pregnant, or no longer follow medication and dietary instructions.

Sites / Locations

  • Imam Reza hospital and clinic of Salamat

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Capsules containing the combination products

Placebo

Arm Description

Capsules containing dog-rose, Cranberry leaves, Cranberry Berries, Alfalfa, Fenugreek, Lemon Beebrush, Urtica, and Sumac

Placebo capsules containing maltodextrin

Outcomes

Primary Outcome Measures

Fasting blood glucose
Change in fasting blood glucose in response to intervention

Secondary Outcome Measures

Insulin level
Change in insulin level in response to intervention
Hemoglobin A1c level
Change in hemoglobin A1c level in response to intervention
High density lipoprotein (HDL) level
Change in high density lipoprotein (HDL) level in response to intervention
Low density lipoprotein (LDL) level
Change in low density lipoprotein (LDL) level in response to intervention
Triglyceride level
Change in triglyceride level in response to intervention
Total cholesterol level
Change in total cholesterol level in response to intervention
Aspartate transaminase level
Change in aspartate transaminase level in response to intervention
Alanine aminotransferase level
Change in alanine aminotransferase level in response to intervention
Blood urea nitrogen level
Change in blood urea nitrogen level in response to intervention
Creatinine level
Change in creatinine level in response to intervention
Prothrombin time
Change in prothrombin time in response to intervention
Bilirubin level
Change in bilirubin level in response to intervention
Ferritin level
Change in ferritin level in response to intervention
Cholinesterase level
Change in cholinesterase level in response to intervention
High-sensitivity C-reactive protein level
Change in high-sensitivity C-reactive protein level in response to intervention

Full Information

First Posted
January 17, 2023
Last Updated
April 11, 2023
Sponsor
Tabriz University of Medical Sciences
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1. Study Identification

Unique Protocol Identification Number
NCT05700513
Brief Title
Dog-rose, Cranberry Leaves, Cranberry Berries, Alfalfa, Fenugreek, Lemon Beebrush, Urtica and Sumac in Diabetes Mellitus
Official Title
The Joint Effects of Dog-rose, Cranberry Leaves, Cranberry Berries, Alfalfa, Fenugreek, Lemon Beebrush, Urtica, and Sumac for Controlling Blood Glucose of Patients With Type II Diabetes Mellitus: A Phase 1-2 Randomized Placebo-Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
July 28, 2023 (Anticipated)
Primary Completion Date
February 28, 2024 (Anticipated)
Study Completion Date
February 28, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Tabriz University of Medical Sciences

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study investigates the safety and combined effect of Cranberry leaves, Cranberry Berries, Alfalfa, Fenugreek, Lemon Beebrush, Urtica, Dog-rose, and Sumac on improving the glycemic profile of patients with type 2 diabetes mellitus compared to the placebo group.
Detailed Description
The present double-blind, randomized and placebo-controlled study will be conducted on type 2 diabetes mellitus patients to evaluate the safety and combined effect of Cranberry leaves, Cranberry Berries, Alfalfa, Fenugreek, Lemon Beebrush, Urtica, Dog-rose, and Sumac on improving glycemic profiles (fasting blood sugar, glycosylated Hemoglobin, 2 hours postprandial blood sugar, insulin concentration, insulin resistance, and beta-cell function). The study also evaluates systolic blood pressure, diastolic blood pressure, anthropometric variables, lipid profile, C-reactive protein, and renal and liver function tests. A pilot study with 30 participants will be conducted to estimate the sample size considering 0.05 first type error and a power of 80%. Individuals aged between 18-70 with a diagnosis of type 2 diabetes mellitus based on WHO criteria for at least one year will be enrolled. Participants will be randomized in the placebo or intervention group to receive two capsules per day before lunch and dinner for six months containing 200 milligrams of equally combined extracts of Cranberry leaves, Cranberry Berries, Alfalfa, Fenugreek, Lemon Beebrush, Urtica, Dog-rose, and Sumac. Participants will be followed up with four office visits (t0= baseline, 1=15th day, 2t=3rd month, 3t=6th month) to assess outcomes. Also, the complications and adherence of patients to intervention will be checked every two weeks by telephonic discussion. The analysis will be performed based on the intent-to-treat method.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Type 2 Diabetes
Keywords
Type 2 diabetes, Insulin resistance, Lipochromin, Vaccinium macrocarpon, Medicago sativa, Trigonella, Fenugreek, Lemon Beebrush, Urtica dioica, Rhus, Sumac

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare Provider
Allocation
Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Capsules containing the combination products
Arm Type
Active Comparator
Arm Description
Capsules containing dog-rose, Cranberry leaves, Cranberry Berries, Alfalfa, Fenugreek, Lemon Beebrush, Urtica, and Sumac
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo capsules containing maltodextrin
Intervention Type
Combination Product
Intervention Name(s)
Capsules containing the combination products
Intervention Description
Capsules containing dog-rose, Cranberry leaves, Cranberry Berries, Alfalfa, Fenugreek, Lemon Beebrush, Urtica, and Sumac
Intervention Type
Drug
Intervention Name(s)
Placebo capsules
Intervention Description
Placebo capsules containing maltodextrin
Primary Outcome Measure Information:
Title
Fasting blood glucose
Description
Change in fasting blood glucose in response to intervention
Time Frame
Day 0, 15, 90, 180 post intervention
Secondary Outcome Measure Information:
Title
Insulin level
Description
Change in insulin level in response to intervention
Time Frame
Day 0, 15, 90, 180 post intervention
Title
Hemoglobin A1c level
Description
Change in hemoglobin A1c level in response to intervention
Time Frame
Day 0, 15, 90, 180 post intervention
Title
High density lipoprotein (HDL) level
Description
Change in high density lipoprotein (HDL) level in response to intervention
Time Frame
Day 0, 15, 90, 180 post intervention
Title
Low density lipoprotein (LDL) level
Description
Change in low density lipoprotein (LDL) level in response to intervention
Time Frame
Day 0, 15, 90, 180 post intervention
Title
Triglyceride level
Description
Change in triglyceride level in response to intervention
Time Frame
Day 0, 15, 90, 180 post intervention
Title
Total cholesterol level
Description
Change in total cholesterol level in response to intervention
Time Frame
Day 0, 15, 90, 180 post intervention
Title
Aspartate transaminase level
Description
Change in aspartate transaminase level in response to intervention
Time Frame
Day 0, 15, 90, 180 post intervention
Title
Alanine aminotransferase level
Description
Change in alanine aminotransferase level in response to intervention
Time Frame
Day 0, 15, 90, 180 post intervention
Title
Blood urea nitrogen level
Description
Change in blood urea nitrogen level in response to intervention
Time Frame
Day 0, 15, 90, 180 post intervention
Title
Creatinine level
Description
Change in creatinine level in response to intervention
Time Frame
Day 0, 15, 90, 180 post intervention
Title
Prothrombin time
Description
Change in prothrombin time in response to intervention
Time Frame
Day 0, 15, 90, 180 post intervention
Title
Bilirubin level
Description
Change in bilirubin level in response to intervention
Time Frame
Day 0, 15, 90, 180 post intervention
Title
Ferritin level
Description
Change in ferritin level in response to intervention
Time Frame
Day 0, 15, 90, 180 post intervention
Title
Cholinesterase level
Description
Change in cholinesterase level in response to intervention
Time Frame
Day 0, 15, 90, 180 post intervention
Title
High-sensitivity C-reactive protein level
Description
Change in high-sensitivity C-reactive protein level in response to intervention
Time Frame
Day 0, 15, 90, 180 post intervention

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: At least one year of diagnosis of type 2 diabetes according to the criteria of the World Health Organization, Hemoglobin A1c (HbA1c) > 7.0% or fasting blood glucose > 7.0 mmol/L, Body mass index (BMI) more than 23 kg/m2 and less than 35. Exclusion Criteria: Comorbidities, including type 1 diabetes, cardiovascular disease, thyroid disease, liver disease, kidney disease, cancer, mental disorders, and the use of drugs related to the aforementioned diseases, Pregnancy, Patients with a BMI over 35 who were on a weight loss diet or had taken weight loss supplements for less than 6 months A history of allergy to one of the components of the nestling fruit, carob leaf, carob fruit, alfalfa seed, fenugreek seed, lemon, Nettles and sumac and also Lactating women Regularly consuming cigarettes or alcohol Using psychiatric drugs or insulin Changing in the medication regimen during the trial period. For example, to start receiving insulin therapy, become pregnant, or no longer follow medication and dietary instructions.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Saeid Safiri, PhD
Phone
+984133342178
Email
saeidsafiri@gmail.com
Facility Information:
Facility Name
Imam Reza hospital and clinic of Salamat
City
Tabriz
State/Province
AzarbayejaneShargi
ZIP/Postal Code
5166614766
Country
Iran, Islamic Republic of

12. IPD Sharing Statement

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Dog-rose, Cranberry Leaves, Cranberry Berries, Alfalfa, Fenugreek, Lemon Beebrush, Urtica and Sumac in Diabetes Mellitus

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