Research on the Blood- Cooling - Toxin - Removing - Stasis - Dispersing Protocol Evaluation of Hench-schonlein Purpura

Liaoning University of Traditional Chinese Medicine

Status and phase

Unknown

Phase 2

Conditions

Purpura, Schoenlein-Henoch

Treatments

Drug: "ziying" granules

Drug: Placebo

Study type

Interventional

Funder types

Other

Identifiers

NCT01104428

zhangjun555678

Details and patient eligibility

About

Due to high incidence of renal damage by Hench-schonlein Purpura(HSP) is the key to affect prognosis, this project moves the research emphasis forward in line with the idea of "prevention of progress of disease", Which concerns on Traditional Chinese Medicine(TCM) clinical research scheme evaluation of HSP, evaluates the renal damage and disease recurrence as the end event, and comes to the evaluation through the comparative study that the vantage point of the scheme of syndrome differentiation and treatment in detoxification, cooling blood and removing blood stasis to the conventional treatments can reduce kidney damage and recurrence rate.

Full description

Target：Optimize the TCM scheme of syndrome differentiation and treatment of HSP in line with the idea of blood- Cooling - Toxin - Removing - Stasis - Dispersing under the path of combination between disease differentiation and syndrome differentiation, and regards reducing the rate of the recurrence of HSP and kidney damage as the end point of evaluation indexes, to evaluate the clinical efficacy of the scheme scientifically. Main research contents: Retrospective case investigation, analysis and research on literature, research on clinical assessment of the scheme of syndrome differentiation and treatment. Methods：With a series of compounds as the main interference factors, choosing the sample estimation of superiority design and adopting the test methods of randomized, double-blind, placebo-controlled to carry out the research of multicenter clinical efficacy evaluation.

It summarizes the advantages and rules of syndrome differentiation and treatment in TCM by means of the comparative study, which provides technical guidelines for the industry and sets an example to summarize the key common technology of clinical research, and also improves the evaluation level of TCM clinical research and efficacy.

Enrollment

256 estimated patients

Sex

All

Ages

5 to 18 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

To comply with the diagnostic standard of purpura in TCM and Hench-schonlein purpura in western medicine;
To comply with the diagnostic standard of TCM syndrome differentiation;
Age between 5 and 18;
without similar herbal treatment a week before being included;
Informed Consent Form is required to be singed.

Exclusion criteria

Fall short of the diagnostic standard of purpura in TCM and Hench-schonlein purpura in western medicine;
Fall short of the diagnostic standard of TCM syndrome differentiation;
Older then 18 years or younger then 5years;
Take similar herbal treatment within a week before being included;
Can not take the drug according to the regulation or follow-up on time
Patients combine serious primary disease in respiratory、gastrointestinal、hemopoietic、renal，or psychosis,or pestilence;
Allergic to drugs of this research or others;
human subject of other clinical research in the nearly tow weeks.