Development The Potentiality of β-1,3/1,6-D-Glucan (Polysaccharide Peptide) From Mycelia Extract of Indonesia's Ganoderma Lucidum as Adjuvant Therapy in Patients With Cardiometabolic Syndrome
Primary Purpose
Cardiometabolic Syndrome
Status
Unknown status
Phase
Phase 2
Locations
Indonesia
Study Type
Interventional
Intervention
β-1,3/1,6-D-Glucan From Mycelia Extract of Indonesia's Ganoderma Lucidum Group
Placebo Group
Sponsored by
About this trial
This is an interventional treatment trial for Cardiometabolic Syndrome focused on measuring β-1,3/1,6-D-Glucan, Polysaccharide Peptide, Ganoderma lucidum, Cardiometabolic syndrome
Eligibility Criteria
Inclusion Criteria:
- Age more or same than 18 years old
- Defined as metabolic syndrome patients based on NCEP-ATP III Criteria with modified of obesity classification (waist measurement) for Asian population
- Agreed to participate in this study
Exclusion Criteria:
- Allergic to Ganoderma lucidum
- Pregnant woman
- Participate in another drug or medical device study
- Waiting for an organ transplantation or have undergone a transplant
- Cancer patients who undergoing a chemotherapy or radiotherapy
- People with organ failure
- Could not be randomized and participate in this study by clinical judgement
Sites / Locations
- General Hospital of Brawijaya University (Rumah Sakit Universitas Brawijaya)
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
β-1,3/1,6-D-Glucan From Mycelia Extract of Indonesia's Ganoderma Lucidum Group
Placebo Group
Arm Description
This group will receive capsule contains 180 mg of β-1,3/1,6-D-Glucan From Mycelia Extract of Indonesia's Ganoderma lucidum which will be taken 3 times daily for 90 days
This group will receive empty capsule which will be taken 3 times daily for 90 days
Outcomes
Primary Outcome Measures
Change in Quality of Life from completion of SF-36 questionnaire
Quality of Life is assessed by Indonesia validated Short Formm 36 questionnaire. This questionnaire consist of 36 items/questions that evaluate quality of life in some elements. The elements are consisted of changes in health (1 item), general health perception (5 items), energy/fatique (4 items), mental health (5 items), social functioning (2 items), pain (2 items), physical functioning (10 items), role limitations due to emotional problems (3 items) and role limitations due to physical problems (4 items).
The score from each question will be summed. Minimum score is 36 and maximum score is 138. Higher score indicates higher quality of life and lower score indicates lower quality of life. Higher score after intervention in post-test examination represents a positive outcome
Secondary Outcome Measures
Change of inflammation status parameter (IL-6) level
Level of IL-6 is obtained from laboratory blood plasma test
Change of inflammation status parameter (TNF-alpha) level
Level of TNF-alpha is obtained from laboratory blood plasma test
Change of inflammation status parameter (hs-CRP) level
Level of hs-CRP is obtained from laboratory blood plasma test
Change of oxidative stress parameter (MDA) level
Level of MDA is obtained from laboratory blood plasma test
Change of oxidative stress parameter (SOD) level
Level of SOD is obtained from laboratory blood plasma test
Change of endothelial function (NO) parameter level
Level of NO is obtained from laboratory blood plasma test
Change of waist circumference measurement
Waist circumference is measured by tape to determine abdominal obesity
Change of body weight and body height measurement
Body weight is measured by body weight scale and body height is measured by body height scale, then will be combined to determine BMI in kg/m^2
Change of blood pressure
Blood pressure is measured using manual sphygmomanometer
Change of fasting glucose level
Fasting glucose level is obtained from laboratory blood test
Change of HbA1C serum level
HbA1C serum level is obtained from laboratory blood test
Change of triglicyride level status
Triglyceride level is obtained from laboratory blood test
Change of total cholesterol level status
Total cholesterol level is obtained from laboratory blood test
Change of HDL level status
HDL level is obtained from laboratory blood test
Change of LDL level status
LDL level is obtained from laboratory blood test
Change of creatinine blood level
Creatinine level is obtained from laboratory blood test
Change of urea blood level
Urea level is obtained from laboratory blood test
Full Information
NCT ID
NCT05079529
First Posted
September 18, 2021
Last Updated
October 3, 2021
Sponsor
University of Brawijaya
Collaborators
PT. Sahabat Lingkungan Hidup
1. Study Identification
Unique Protocol Identification Number
NCT05079529
Brief Title
Development The Potentiality of β-1,3/1,6-D-Glucan (Polysaccharide Peptide) From Mycelia Extract of Indonesia's Ganoderma Lucidum as Adjuvant Therapy in Patients With Cardiometabolic Syndrome
Official Title
Development The Potentiality of β-1,3/1,6-D-Glucan (Polysaccharide Peptide) From Mycelia Extract of Indonesia's Ganoderma Lucidum as Adjuvant Therapy in Patients With Cardiometabolic Syndrome Based on NCEP-ATP III Criteria With Modification on Obesity Classification (Waist Circumference Measurement) for Asian Population
Study Type
Interventional
2. Study Status
Record Verification Date
October 2021
Overall Recruitment Status
Unknown status
Study Start Date
June 30, 2021 (Actual)
Primary Completion Date
December 28, 2021 (Anticipated)
Study Completion Date
January 6, 2022 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Brawijaya
Collaborators
PT. Sahabat Lingkungan Hidup
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
The aim of this study is to determine the role and efficacy of β-1,3/1,6-D-Glucan (Polysaccharide Peptide) from mycelia extract of Indonesia's Ganoderma lucidum as an antioxidant and anti-inflammatory agent on cardiometabolic syndrome
Detailed Description
This study is held at Saiful Anwar General Hospital and General Hospital of Brawijaya University by enrolled 70 participants and using a double-blinded true experimental using a randomized control perspective method with pre-test and post-test design, to determine the effect of giving β-1,3/1,6-D-Glucan (Polysaccharide Peptide) from mycelia extract of Indonesia's Ganoderma lucidum on cardiometabolic syndrome population.
The intended target or experimental variables that will be studied in this study are blood pressure, body mass index, blood glucose profile (fasting glucose, HbA1C), lipid profile (total cholesterol, High-Density Lipoprotein, Low-Density Lipoprotein, and triglyceride), renal function profile (urea and creatinine), heart function from echocardiography examination, inflammation parameter (Interleukin 6, Tumor Necrosis Factor-Alpha, and high sensitivity C-Reactive Protein), stress oxidative parameter (superoxide dismutase and malondialdehyde), endothelial function parameter (nitric oxide), and quality of life that conducted by completion of the SF-36 questionnaire.
Hypothesis of this study is β-1,3/1,6-D-Glucan (Polysaccharide Peptide) from mycelia extract of Indonesia's Ganoderma lucidum can acts as a chronic anti-inflammatory and antioxidant agent in cardiometabolic syndrome patients by contributing in blood pressure control, body mass index control, blood glucose improvement, lipid profile improvement, renal function profile improvement, heart function improvement, and better quality of life. Beside that, the investigators hope that there will be a change of inflammation, stress oxidative, and endothelial function parameter in which shift to the good level.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cardiometabolic Syndrome
Keywords
β-1,3/1,6-D-Glucan, Polysaccharide Peptide, Ganoderma lucidum, Cardiometabolic syndrome
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Model Description
This study conducted cardiometabolic syndrome patients based on NCEP-ATPIII criteria with modification of obesity classification to Asian population criteria. All of the participant would be divided into 2 groups/arms in which one group will be given Polysaccharide Peptide capsule 3 times daily for 90 days and the other one will be given Placebo in the same duration of time.
Before Polysaccharide Peptide is given, there will be a sequence of pre-test examination, include: blood pressure measurement, body weight and body height measurement to determine Body Mass Index status, waist circumference measurement, blood glucose profile, lipid profile, renal function profile, parameter of inflammation status, parameter of oxidative stress, parameter of endothelial function, and completion of SF 36 questionnaire in which all of them will be done as post-test after intervention completed.
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Masking Description
This study is randomized control double-blinded true experimental study. So the only party that acknowledge whom is given Polysaccharide Peptide capsule or Placebo is the collaborator who provides the adjuvant therapy agent. There is an exception for Outcomes Assessor. They might ask for detail description of the intervention that have been given to the participant if there is any serious adverse event going on.
Allocation
Randomized
Enrollment
70 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
β-1,3/1,6-D-Glucan From Mycelia Extract of Indonesia's Ganoderma Lucidum Group
Arm Type
Experimental
Arm Description
This group will receive capsule contains 180 mg of β-1,3/1,6-D-Glucan From Mycelia Extract of Indonesia's Ganoderma lucidum which will be taken 3 times daily for 90 days
Arm Title
Placebo Group
Arm Type
Placebo Comparator
Arm Description
This group will receive empty capsule which will be taken 3 times daily for 90 days
Intervention Type
Drug
Intervention Name(s)
β-1,3/1,6-D-Glucan From Mycelia Extract of Indonesia's Ganoderma Lucidum Group
Other Intervention Name(s)
β-1,3/1,6-D-Glucan
Intervention Description
Takes β-1,3/1,6-D-Glucan capsule 3 times daily for 90 days
Intervention Type
Drug
Intervention Name(s)
Placebo Group
Intervention Description
Takes placebo capsule 3 times daily for 90 days
Primary Outcome Measure Information:
Title
Change in Quality of Life from completion of SF-36 questionnaire
Description
Quality of Life is assessed by Indonesia validated Short Formm 36 questionnaire. This questionnaire consist of 36 items/questions that evaluate quality of life in some elements. The elements are consisted of changes in health (1 item), general health perception (5 items), energy/fatique (4 items), mental health (5 items), social functioning (2 items), pain (2 items), physical functioning (10 items), role limitations due to emotional problems (3 items) and role limitations due to physical problems (4 items).
The score from each question will be summed. Minimum score is 36 and maximum score is 138. Higher score indicates higher quality of life and lower score indicates lower quality of life. Higher score after intervention in post-test examination represents a positive outcome
Time Frame
0 and 90 days
Secondary Outcome Measure Information:
Title
Change of inflammation status parameter (IL-6) level
Description
Level of IL-6 is obtained from laboratory blood plasma test
Time Frame
0 and 90 days
Title
Change of inflammation status parameter (TNF-alpha) level
Description
Level of TNF-alpha is obtained from laboratory blood plasma test
Time Frame
0 and 90 days
Title
Change of inflammation status parameter (hs-CRP) level
Description
Level of hs-CRP is obtained from laboratory blood plasma test
Time Frame
0 and 90 days
Title
Change of oxidative stress parameter (MDA) level
Description
Level of MDA is obtained from laboratory blood plasma test
Time Frame
0 and 90 days
Title
Change of oxidative stress parameter (SOD) level
Description
Level of SOD is obtained from laboratory blood plasma test
Time Frame
0 and 90 days
Title
Change of endothelial function (NO) parameter level
Description
Level of NO is obtained from laboratory blood plasma test
Time Frame
0 and 90 days
Title
Change of waist circumference measurement
Description
Waist circumference is measured by tape to determine abdominal obesity
Time Frame
0 and 90 days
Title
Change of body weight and body height measurement
Description
Body weight is measured by body weight scale and body height is measured by body height scale, then will be combined to determine BMI in kg/m^2
Time Frame
0 and 90 days
Title
Change of blood pressure
Description
Blood pressure is measured using manual sphygmomanometer
Time Frame
0 and 90 days
Title
Change of fasting glucose level
Description
Fasting glucose level is obtained from laboratory blood test
Time Frame
0 and 90 days
Title
Change of HbA1C serum level
Description
HbA1C serum level is obtained from laboratory blood test
Time Frame
0 and 90 days
Title
Change of triglicyride level status
Description
Triglyceride level is obtained from laboratory blood test
Time Frame
0 and 90 days
Title
Change of total cholesterol level status
Description
Total cholesterol level is obtained from laboratory blood test
Time Frame
0 and 90 days
Title
Change of HDL level status
Description
HDL level is obtained from laboratory blood test
Time Frame
0 and 90 days
Title
Change of LDL level status
Description
LDL level is obtained from laboratory blood test
Time Frame
0 and 90 days
Title
Change of creatinine blood level
Description
Creatinine level is obtained from laboratory blood test
Time Frame
0 and 90 days
Title
Change of urea blood level
Description
Urea level is obtained from laboratory blood test
Time Frame
0 and 90 days
Other Pre-specified Outcome Measures:
Title
Number of participants with adverse event (AEs)
Description
Number of participants that experience adverse event in this study
Time Frame
30, 60, and 90 days
Title
Number of participants with Serious Adverse Event (SAEs)
Description
Number of participants that go through serious adverse event in this study
Time Frame
30, 60, and 90 days
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age more or same than 18 years old
Defined as metabolic syndrome patients based on NCEP-ATP III Criteria with modified of obesity classification (waist measurement) for Asian population
Agreed to participate in this study
Exclusion Criteria:
Allergic to Ganoderma lucidum
Pregnant woman
Participate in another drug or medical device study
Waiting for an organ transplantation or have undergone a transplant
Cancer patients who undergoing a chemotherapy or radiotherapy
People with organ failure
Could not be randomized and participate in this study by clinical judgement
Facility Information:
Facility Name
General Hospital of Brawijaya University (Rumah Sakit Universitas Brawijaya)
City
Malang
State/Province
East Java
ZIP/Postal Code
65141
Country
Indonesia
12. IPD Sharing Statement
Plan to Share IPD
Undecided
IPD Sharing Plan Description
The research team would like to discuss to what extent and the criteria of individual participant data that will be shared related to Statistical Analysis Plan, Informed Consent Form and/or Clinical Study Report
Citations:
PubMed Identifier
25136585
Citation
Dinh QN, Drummond GR, Sobey CG, Chrissobolis S. Roles of inflammation, oxidative stress, and vascular dysfunction in hypertension. Biomed Res Int. 2014;2014:406960. doi: 10.1155/2014/406960. Epub 2014 Jul 20.
Results Reference
result
PubMed Identifier
26131326
Citation
Kharroubi AT, Darwish HM. Diabetes mellitus: The epidemic of the century. World J Diabetes. 2015 Jun 25;6(6):850-67. doi: 10.4239/wjd.v6.i6.850.
Results Reference
result
Links:
URL
https://austinpublishinggroup.com/cardiovascular-diseases/fulltext/ajcd-v3-id1017.php
Description
Journal Title: Vascular Inflammation and Hypertension
URL
https://www.google.com/url?sa=t&rct=j&q=&esrc=s&source=web&cd=&cad=rja&uact=8&ved=2ahUKEwjt-4mj36_zAhUS5nMBHaFQCYsQFnoECAkQAQ&url=https%3A%2F%2Fcare.diabetesjournals.org%2Fcontent%2Fdiacare%2Fsuppl%2F2016%2F12%2F15%2F40.Supplement_1.DC1%2FDC_40_S1_final.pdf&usg=AOvVaw0Qzl4wVSDwGETFGIa99gJB
Description
Standards of Medical Care in Diabetes
URL
https://www.google.com/url?sa=t&rct=j&q=&esrc=s&source=web&cd=&cad=rja&uact=8&ved=2ahUKEwjt_eG636_zAhVj5nMBHZexBdkQFnoECAkQAQ&url=https%3A%2F%2Fwww.longdom.org%2Fopen-access%2Fclassification-pathophysiology-diagnosis-and-management-of-diabetesmellitus-2155-6156-1000541.pdf&usg=AOvVaw3TEJc1UhMPP5_lZDYF-Y1z
Description
Journal Title: Pathophysiology, Diagnosis and Management of Diabetes Melitus
URL
https://www.google.com/url?sa=t&rct=j&q=&esrc=s&source=web&cd=&cad=rja&uact=8&ved=2ahUKEwi5lYHY36_zAhWtuksFHUGjCH8QFnoECAMQAQ&url=https%3A%2F%2Fwww.iomcworld.org%2Fopen-access%2Fhypertension-pathophysiology-and-treatment-2155-9562-5-1000250.pdf&usg=AOvVaw2rNOEbO3b_BS9WrpNQHWVx
Description
Journal Title: Hypertension: Pathophysiology and Treatment
URL
https://www.cdc.gov/mmwr/volumes/65/wr/mm6545a3.htm
Description
CDC Grand Rounds: A Public Health Approach to Detect and Control Hypertension
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Development The Potentiality of β-1,3/1,6-D-Glucan (Polysaccharide Peptide) From Mycelia Extract of Indonesia's Ganoderma Lucidum as Adjuvant Therapy in Patients With Cardiometabolic Syndrome
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