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Clinical Study of Tang Wang Prescription Intervene Diabetic Non-proliferative Retinopathy

Primary Purpose

Diabetic Non-proliferative Retinopathy, Type2 Diabetes

Status
Unknown status
Phase
Early Phase 1
Locations
Study Type
Interventional
Intervention
Tangwang prescription
Placebo
Sponsored by
Fengmei Lian
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diabetic Non-proliferative Retinopathy focused on measuring tang wang prescription

Eligibility Criteria

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

Inclusion Criteria:

  1. Diagnosis of diabetic retinopathy、the degree of disease was non-proliferative diabetic retinopathy;
  2. Age at 30-70 years old;
  3. Signed the informed consent;

    • Note: Diabetic retinopathy patients can be selected as the observation object, Who only one eye can meet the inclusion criteria, If both eyes of patient can be selected, please record respectively, and choose one eye to evaluate the curative effect, the eye must according to the following principles: choose the heavier eye as the observation eye, When the fundus conditions of the eyes are in different clinical stages; Select the eye as the eye of clinical manipulation. Choose the eyes with better clinical operation as the observation eyes, When the fundus conditions of the eyes are in same clinical stages.

Exclusion Criteria:

  1. The patients with retinal photocoagulation、appropriate patients for retinal photocoagulation、patient have one or two eyes in diabetic retinopathy proliferative phase、type I diabetes mellitus、there are other eye disease complications(such as glaucoma、cataracts can Significantly interfere the fundus examination、Non - diabetic retinopathy、uveitis、amotio retinae、optic nerve diseases and high myopia with fundus lesions et al.)
  2. Combined with severe primary disease such as cardiovascular、liver、kidney and hematopoietic system et al、the serum transaminase was 2 times larger than the normal valuet、Serum creatinine greater than the upper limit of normal value、Psychiatric patients.
  3. Women with Pregnancy or prepare for pregnancy or lactating.
  4. Patient participated in other clinical researchers within a month.
  5. Patients have been treated with other drugs to treat diabetic retinopathy except for calcium hydroxide within a week.
  6. Systolic blood pressure > 160mmHg or diastolic blood pressure > 100mmHg.
  7. Patients with diabetic ketosis, ketoacidosis and severe infections within a month
  8. Patients have been alcohol abused and / or used psychoactive substances or drug abused or drug addicted within 5 years.
  9. According to the researcher's judgment, patients have Other lesions or conditions maybe reduce the possibility of entering groups or make the groups complex,such as working environment change frequently、Living environment is unstable what easy to cause loss to follow-up.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Placebo Comparator

    Arm Label

    Tangwang Prescription

    Placebo

    Arm Description

    The prescription was composed five Chinese herbal medicines,every bag has 4.87g granules, take it one bag each time, two times a day.

    Placebo is a simulated drug of tangwang Prescription,every bag has 4.87g granules, take it one bag each time, two times a day.

    Outcomes

    Primary Outcome Measures

    the changes of degree of retinal microvascular lesions before and after treatment (no, mild non proliferative phase, moderate non proliferative phase, severe non proliferative phase, proliferative phase)

    Secondary Outcome Measures

    Change of the number of micro hemangioma of diabetic retinopathy
    Change of the number of microvascular bleeding of diabetic retinopathy
    Color fundus photography and fundus fluorescein angiography were performed
    Change of the number of microvascular leakage of diabetic retinopathy
    Degree of change of macular edema of diabetic retinopathy,analysis of measured values of the shortest distance from the margin of edema and the retinal thickness in macular region before and after medication
    Change of Vision (analysis of visual acuity before and after medication using EDTRS international visual acuity chart)

    Full Information

    First Posted
    January 4, 2017
    Last Updated
    January 19, 2017
    Sponsor
    Fengmei Lian
    Collaborators
    Guang'anmen Hospital of China Academy of Chinese Medical Sciences, The First Affiliated Hospital of Anhui University of Traditional Chinese Medicine, Hubei Hospital of Traditional Chinese Medicine, Zhengzhou City Hospital of Traditional Chinese Medicine, Baodin City Hospital of Traditional Chinese Medicine, zi bo wanjie cancer hospital, Shijiazhuang City Hospital of Traditional Chinese Medicine, Zouping Country Hospital of Traditional Chinese Medicine
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    1. Study Identification

    Unique Protocol Identification Number
    NCT03025399
    Brief Title
    Clinical Study of Tang Wang Prescription Intervene Diabetic Non-proliferative Retinopathy
    Official Title
    Multi Center Clinical Study of Chinese Medicine Intervention on Early Diabetic Microvascular Complications: Multi Centers Clinical Study of Tang Wang Prescription Intervene Diabetic Non-proliferative Retinopathy
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    January 2017
    Overall Recruitment Status
    Unknown status
    Study Start Date
    February 2017 (Anticipated)
    Primary Completion Date
    May 2019 (Anticipated)
    Study Completion Date
    May 2020 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor-Investigator
    Name of the Sponsor
    Fengmei Lian
    Collaborators
    Guang'anmen Hospital of China Academy of Chinese Medical Sciences, The First Affiliated Hospital of Anhui University of Traditional Chinese Medicine, Hubei Hospital of Traditional Chinese Medicine, Zhengzhou City Hospital of Traditional Chinese Medicine, Baodin City Hospital of Traditional Chinese Medicine, zi bo wanjie cancer hospital, Shijiazhuang City Hospital of Traditional Chinese Medicine, Zouping Country Hospital of Traditional Chinese Medicine

    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 include 384 Participants with diabetic non-proliferative retinopathy Design Method: Randomized, double blind, placebo controlled and multicenter clinical study. Participants treatment for 48 weeks, and main aimed to evaluate the therapeutic effect of tang wang prescription improve degree of retinal microvascular disease of patients with diabetic non-proliferative retinopathy.
    Detailed Description
    This study is a randomized, double-blinded, placebo-controlled and multicenter clinical trial on type 2 diabetic non-proliferative retinopathy to evaluate the therapeutic effect of tang wang prescription. Through the calculation of sample size, 384 participants with type 2 diabetic non-proliferative retinopathy will be recruited for the study, all participants were randomly divided into 2 groups, and both of groups would be performed on a basic treatment (including diabetes education, diabetes diet, rational control of blood glucose (oral hypoglycemic agents or insulin injections to keep all participants keep blood glucose stable in the study. If fasting blood glucose fluctuates more than 20%, need to find and remove the factors as soon as possible, and adjust the dose and monitor change of blood glucose, make it smooth in 4 weeks. Adjusted dose of the drug needs to be detailed records in the combined medication table), and oral calcium dobesilate treatment), study group take tang wang prescription, take one bag each time and twice on day, control group take the same dose of placebo. The study will last for 48 weeks. Once every four weeks follow-up, color fundus photography, fundus fluorescein angiography, and coherent optical tomography were performed every six months; ETDRS international visual acuity test was performed every months. Curative effect evaluation criteria: Main evaluation criteria: the changes of degree of retinal microvascular lesions before and after treatment, according to the change of degree of retinal microvascular lesions (no, mild non proliferative phase, moderate non proliferative phase, severe non proliferative phase, proliferative phase), divided into aggravated, unchanged, reduce three conditions. Aggravated was defined as the degree of retinal microvascular lesions severity more than grade 1 after treatment; unchanged was defined as the degree of retinal microvascular lesions before and after treatment did not change; reduce was defined as the degree of retinal microvascular lesions reduced more than 1 grade after treatment. Second evaluation criteria: Change of the number of micro hemangioma of diabetic retinopathy before and after treatment; Change of the number of microvascular bleeding of diabetic retinopathy before and after treatment; Change of the number of microvascular leakage of diabetic retinopathy before and after treatment; Degree of change of macular edema of diabetic retinopathy before and after treatment; Change of Vision before and after treatment. Diagnostic and monitoring indicators:blood pressure, fasting blood glucose test (every one month); glycated hemoglobin, blood lipids (every three months); Routine eye examination and fundus examination, including intraocular pressure, anterior segment, lens, vitreous body, and lens, vitreous need describe the conditions of opacity (every six months). The provisions of the combined therapy All Chinese herbal medicines with the same efficacy as the study drug (including Chinese herbal medicines with similar therapeutic and similar efficacy in Instructions) were banned during the study period. All combined therapy and Combined medication(treatment measure or treatment medicine of other diseases) should be recorded in the combined medication table.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Diabetic Non-proliferative Retinopathy, Type2 Diabetes
    Keywords
    tang wang prescription

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Early Phase 1
    Interventional Study Model
    Parallel Assignment
    Masking
    ParticipantInvestigator
    Allocation
    Randomized
    Enrollment
    384 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Tangwang Prescription
    Arm Type
    Experimental
    Arm Description
    The prescription was composed five Chinese herbal medicines,every bag has 4.87g granules, take it one bag each time, two times a day.
    Arm Title
    Placebo
    Arm Type
    Placebo Comparator
    Arm Description
    Placebo is a simulated drug of tangwang Prescription,every bag has 4.87g granules, take it one bag each time, two times a day.
    Intervention Type
    Drug
    Intervention Name(s)
    Tangwang prescription
    Other Intervention Name(s)
    Tang Wang Fang
    Intervention Description
    A kind of Granule(Tangwang prescription) was composition by five Chinese herbal medicines, every bag has 4.87g granules.
    Intervention Type
    Drug
    Intervention Name(s)
    Placebo
    Other Intervention Name(s)
    Placebos
    Intervention Description
    Placebo is a simulated drug of tangwang prescription,included weight, appearance, colour, taste,smell and solubility.
    Primary Outcome Measure Information:
    Title
    the changes of degree of retinal microvascular lesions before and after treatment (no, mild non proliferative phase, moderate non proliferative phase, severe non proliferative phase, proliferative phase)
    Time Frame
    0 week, 24 weeks, 48 weeks
    Secondary Outcome Measure Information:
    Title
    Change of the number of micro hemangioma of diabetic retinopathy
    Time Frame
    0 week, 24 weeks, 48 weeks
    Title
    Change of the number of microvascular bleeding of diabetic retinopathy
    Description
    Color fundus photography and fundus fluorescein angiography were performed
    Time Frame
    0 week, 24 weeks, 48 weeks
    Title
    Change of the number of microvascular leakage of diabetic retinopathy
    Time Frame
    0 week, 24 weeks, 48 weeks
    Title
    Degree of change of macular edema of diabetic retinopathy,analysis of measured values of the shortest distance from the margin of edema and the retinal thickness in macular region before and after medication
    Time Frame
    0 week, 24 weeks, 48 weeks
    Title
    Change of Vision (analysis of visual acuity before and after medication using EDTRS international visual acuity chart)
    Time Frame
    0 week, 4 weeks, 8 weeks,12 weeks,16 weeks, 20 weeks, 24 weeks, 28 weeks, 32 weeks, 36 weeks, 40 weeks, 44 weeks, 48 weeks

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    30 Years
    Maximum Age & Unit of Time
    70 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Diagnosis of diabetic retinopathy、the degree of disease was non-proliferative diabetic retinopathy; Age at 30-70 years old; Signed the informed consent; Note: Diabetic retinopathy patients can be selected as the observation object, Who only one eye can meet the inclusion criteria, If both eyes of patient can be selected, please record respectively, and choose one eye to evaluate the curative effect, the eye must according to the following principles: choose the heavier eye as the observation eye, When the fundus conditions of the eyes are in different clinical stages; Select the eye as the eye of clinical manipulation. Choose the eyes with better clinical operation as the observation eyes, When the fundus conditions of the eyes are in same clinical stages. Exclusion Criteria: The patients with retinal photocoagulation、appropriate patients for retinal photocoagulation、patient have one or two eyes in diabetic retinopathy proliferative phase、type I diabetes mellitus、there are other eye disease complications(such as glaucoma、cataracts can Significantly interfere the fundus examination、Non - diabetic retinopathy、uveitis、amotio retinae、optic nerve diseases and high myopia with fundus lesions et al.) Combined with severe primary disease such as cardiovascular、liver、kidney and hematopoietic system et al、the serum transaminase was 2 times larger than the normal valuet、Serum creatinine greater than the upper limit of normal value、Psychiatric patients. Women with Pregnancy or prepare for pregnancy or lactating. Patient participated in other clinical researchers within a month. Patients have been treated with other drugs to treat diabetic retinopathy except for calcium hydroxide within a week. Systolic blood pressure > 160mmHg or diastolic blood pressure > 100mmHg. Patients with diabetic ketosis, ketoacidosis and severe infections within a month Patients have been alcohol abused and / or used psychoactive substances or drug abused or drug addicted within 5 years. According to the researcher's judgment, patients have Other lesions or conditions maybe reduce the possibility of entering groups or make the groups complex,such as working environment change frequently、Living environment is unstable what easy to cause loss to follow-up.
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Fengmei Lian, PHD
    Phone
    0086-010-88001402
    Email
    lfm565@sohu.com

    12. IPD Sharing Statement

    Plan to Share IPD
    Undecided
    Citations:
    PubMed Identifier
    33790783
    Citation
    Jin D, Zhang Y, Zhang Y, Huang W, Meng X, Yang F, Bao Q, Zhang M, Yang Y, Ni Q, Lian F, Tong X. Efficacy and Safety of TangWang Prescription for Type 2 Non-Proliferative Diabetic Retinopathy: A Study Protocol for a Randomized Controlled Trial. Front Pharmacol. 2021 Mar 15;12:594308. doi: 10.3389/fphar.2021.594308. eCollection 2021.
    Results Reference
    derived

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    Clinical Study of Tang Wang Prescription Intervene Diabetic Non-proliferative Retinopathy

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