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WithdrawnNCT01680055Updated Apr 20, 2016

Collection of Blood and Bone Marrow From Patients With Aplastic Anemia for Analysis of Adhesion Molecules, Chemokines and Their Receptors

An observational study in Aplastic Anemia and Healthy, sponsored by Shandong University. Withdrawn at 1 site in China. Open to participants aged 16 Years to 70 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2016-04-20.

Sponsored by Shandong University · Observational

Why this study was withdrawn
No eligible patient was enrolled.
Study type
Observational
Model
Case-control
Time perspective
Prospective
Enrollment
0
Ages
16 Years to 70 Years
Sex
All
01

Study summary

This study is designed to collect bone marrow and/or peripheral blood cells and plasma, for the analysis of adhesion molecules, chemokines and their receptors from newly-diagnosed aplastic anemia patients, and patients treated with antithymocyte globulin plus cyclosporine

02

Conditions studied

  • Aplastic Anemia
  • Healthy
03

In context

Anemia

1,733 studies on the registry are indexed under Anemia; 246 are open to participants now.

Browse Anemia studies →

Lead sponsor

Shandong University is the lead sponsor of 284 studies on the registry; 59 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
16 Years to 70 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Probability sample

Study population

Patients With Aplastic Anemia

Inclusion criteria

  • patients who fulfilled entry criteria of acquired aplastic anemia age range 16-70 years

Exclusion criteria

Exclusion Criteria:

  • Patients complicated with diabetes, tumor, pregnancy, active infection, or connective tissue diseases, such as systemic lupus erythematosus.
05

Study design

Observational model
Case-control
Time perspective
Prospective
Enrollment
0 participants (actual)

Groups and cohorts

  • AA-ATG

    Acquired Aplastic Anemia Patients Treated with Antithymocyte Globulin plus Cyclosporine

06

What researchers measure

Primary outcomes

  1. hematologic response

    hematologic response at 6 months following antithymocyte globulin plus cyclosporine treatment, defined as no longer meeting the criteria for severe aplastic anemia

    Time frame: 6 months following antithymocyte globulin plus cyclosporine treatment

07

Study locations

1 site
  • Qilu Hospital, Shandong University
    Jinan, Shandong 250012, China
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 20, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01680055
Lead sponsor
Shandong University
Responsible party
Ming Hou (Director, Shandong University) — Principal investigator
First posted
Sep 6, 2012
Start date
Feb 2009
Completion
Nov 2012 (estimated)
Last update
Apr 20, 2016
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is withdrawn, as verified in Sep 2012. You cannot join it, but the record below documents what was studied.

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