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

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

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01104428
Enrollment
256
Registered
2010-04-15
Start date
2009-11-30
Completion date
Unknown
Last updated
2010-09-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Purpura, Schoenlein-Henoch

Keywords

Hench-schonlein purpura, Renal damage, Relapse, End event, TCM syndrome

Brief summary

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.

Detailed 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.

Interventions

DRUGPlacebo

granules, \<10years,10g,Three times a day,take orally \>10years,20g,Three times a day,take orally fore weeks a period,Observe 2 periods

DRUGziying granules

granules, \<10years,10g,Three times a day,take orally \>10years,20g,Three times a day,take orally fore weeks a period,Observe 2 periods

Sponsors

Dongzhimen Hospital, Beijing
CollaboratorOTHER
Shenyang Hospital of Integrated Traditional and westen Medicine
CollaboratorUNKNOWN
Dalian Children's Hospital
CollaboratorOTHER
Liaoning University of Traditional Chinese Medicine
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
5 Years to 18 Years
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
whether endpoint such as renal damage or disease recurrence appears in the participants.6 monthsEndpoint is a mark of termination or completion. In this clinical research, the renal damage and disease recurrence that constitutes the target outcomes of the trial.

Secondary

MeasureTime frameDescription
whether the TCM syndrome of participants disappears after treatment.1 monthOptimize 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 In the process of disease of a series of function, metabolism and morphological structure changes caused by the subjective feeling of abnormal patient as symptoms.

Countries

China

Contacts

Primary Contactzhang shaoqing, Master
yanzi8164@163.com86-024-86291599
Backup Contactyang guanqi, Master
86-024-86291599

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026