NCT03681704

Brief Summary

Efficacy and Safety of treatment with Traditional Chinese Medicine HuangQi Decoctions in Patients with early stage of Diabetic Kidney Disease.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
96

participants targeted

Target at P75+ for phase_1

Timeline
Completed

Started Nov 2018

Typical duration for phase_1

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

September 11, 2018

Completed
13 days until next milestone

First Posted

Study publicly available on registry

September 24, 2018

Completed
2 months until next milestone

Study Start

First participant enrolled

November 8, 2018

Completed
3.1 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2021

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2021

Completed
Last Updated

May 11, 2022

Status Verified

May 1, 2022

Enrollment Period

3.1 years

First QC Date

September 11, 2018

Last Update Submit

May 5, 2022

Conditions

Keywords

Diabetic Kidney Disease,Traditional Chinese medicine

Outcome Measures

Primary Outcomes (1)

  • ACR

    the Urinary albumin/ creatinine ratios in stage Ⅲ diabetes kidney disease patients

    24 weeks

Study Arms (2)

HuangQi Decoction

EXPERIMENTAL

HuangQi Decoction 150ml by mouth ,twice a day for 24 weeks

Drug: HuangQi Decoction

HuangQi Decoction placebo

PLACEBO COMPARATOR

HuangQi Decoction placebo 150ml by mouth, twice a day for 24 weeks

Drug: HuangQi Decoction placebo

Interventions

HuangQi Decoction 150ml twice a day for 24 weeks

Also known as: Astragalus and other TCMs Decoction
HuangQi Decoction

traditional Chinese medicine placebo mimic HuangQi Decoction 150ml twice a day for 24 weeks

Also known as: Astragalus Decoction placebo
HuangQi Decoction placebo

Eligibility Criteria

Age18 Years - 75 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Identify the diagnosis of type 2 diabetes;
  • It meets the medical history of diabetic kidney disease, according to the Mogensen diagnostic staging standard DKD III;
  • Age 18-75 years old, gender &ethnicity are not limited;
  • glycated hemoglobin ≤ 10%;
  • Blood pressure is controlled below 130/80mmHg

You may not qualify if:

  • Combine other ACEI and ARB application indications other than hypertension;
  • Combine severe primary diseases related to heart, brain, liver and hematopoietic system;
  • Patients who have acute metabolic disorders such as diabetic ketoacidosis occur in the past month;
  • Patients who HBV serological indicators except HbsAb are positive and persistent liver function test transaminase abnormalities;
  • Patients with malignant tumors or history of malignant tumors, history of HIV infection, history of psychosis, acute central nervous system diseases, severe gastrointestinal diseases, and banned use of immunosuppressive agents;
  • Patients with acute renal failure, combined with urinary tract infection, menstrual period, intense exercise, cold and other stress states;
  • pregnant or lactating women;
  • Patients who accepted other clinical trial studies on going ;
  • Patients who combined with serious diseases and dysfunctions in other organs.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Longhua Hospital, Shanghai University of Traditional Chinese Medicine

Shanghai, Shanghai Municipality, 200032, China

Location

MeSH Terms

Interventions

huangqi decoction

Study Officials

  • Yueyi Deng, PhD

    Shanghai University of Traditional Chinese Medicine

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
phase 1
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, INVESTIGATOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

September 11, 2018

First Posted

September 24, 2018

Study Start

November 8, 2018

Primary Completion

December 31, 2021

Study Completion

December 31, 2021

Last Updated

May 11, 2022

Record last verified: 2022-05

Locations