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Treatment for HBV-MN Patients in Chinese: An Open Parallel Controlled Trial

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified May 2010 by Nanchang University.
Recruitment status was:  Active, not recruiting
ClinicalTrials.gov Identifier:
First Posted: June 29, 2010
Last Update Posted: June 29, 2010
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
Nanchang University
Lamivudine treatment for HBV-DNA negative HBV-GN patients.

Proteinuria HBVe-antigen

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective
Official Title: an Open Parallel Clinical Trial in HBV-GN Patients

Further study details as provided by Nanchang University:

Biospecimen Retention:   Samples Without DNA
not available

Estimated Enrollment: 10
Study Start Date: January 2010
Estimated Study Completion Date: November 2010
Estimated Primary Completion Date: November 2010 (Final data collection date for primary outcome measure)
prednisone and anti-virus

Detailed Description:
lamivudine and predinisone treatment for HBV-DNA negative HBV-GN patients.

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 60 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population
HBV-MN patients with heavy proteinuria in adults; HBsAg or HBeAg positive; HBV-DNA negative

Inclusion Criteria:

  • Adult HBV-GN patients with biopsy-proven MN, heavy protinuria, HBsAg or HBeAg positive, HBV-DNA negative

Exclusion Criteria:

  • Primary MN patients, HBV-DNA positive
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01152060

Sponsors and Collaborators
Nanchang University
Study Director: Gaosi XU, MD & PhD second affiliated hospital to nanchang university
  More Information

Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: ethics committee of Nanchang University, second affiliated hospital
ClinicalTrials.gov Identifier: NCT01152060     History of Changes
First Submitted: June 28, 2010
First Posted: June 29, 2010
Last Update Posted: June 29, 2010
Last Verified: May 2010

Keywords provided by Nanchang University:
remission of proteinuria

Additional relevant MeSH terms:
Urination Disorders
Urologic Diseases
Urological Manifestations
Signs and Symptoms
Anti-Inflammatory Agents
Hormones, Hormone Substitutes, and Hormone Antagonists
Physiological Effects of Drugs
Antineoplastic Agents, Hormonal
Antineoplastic Agents