High-dose Dexamethasone Versus Conventional Dose Prednisone for Initial Treatment of Primary Immune Thrombocytopenia (ITP)

NCT01356511 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 261

Last updated 2016-04-20

No results posted yet for this study

Summary

The project was undertaking by Qilu Hospital of Shandong University and other 11 well-known hospitals in China. In order to report the efficacy and safety of high-dose dexamethasone compared to conventional dose prednisone for the first-line treatment of adults with primary immune thrombocytopenia(ITP).

Conditions

  • Purpura, Thrombocytopenic, Idiopathic

Interventions

DRUG

Prednisone

Prednisone, po, 1 mg/kg/d, for 4 weeks.

DRUG

Dexamethasone

Dexamethasone, po, 40 mg/d, for 4 days.

Sponsors & Collaborators

  • Chinese Academy of Medical Sciences

    collaborator OTHER
  • Peking Union Medical College Hospital

    collaborator OTHER
  • Ruijin Hospital

    collaborator OTHER
  • Union Hospital, Tongji Medical College, Huazhong University of Science and Technology

    collaborator OTHER
  • Tongji Hospital

    collaborator OTHER
  • Shandong University of Traditional Chinese Medicine

    collaborator OTHER
  • Anhui Provincial Hospital

    collaborator OTHER_GOV
  • Zhejiang Provincial Hospital of TCM

    collaborator OTHER
  • Second Hospital of Shanxi Medical University

    collaborator OTHER
  • People's Hospital of Xinjiang Uygur Autonomous Region

    collaborator OTHER
  • Shenzhen Second People's Hospital

    collaborator OTHER
  • Shandong University

    lead OTHER

Principal Investigators

  • Ming Hou, DR. · Shandong University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-09-30
Primary Completion
2014-05-31
Completion
2015-03-31

Countries

  • China

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01356511 on ClinicalTrials.gov