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FCM Analysis GR in Steroid-Treatment Patients

Flow Cytometric Analysis of Glucocorticoid Receptor Using Monoclonal Antibody and Fluoresceinated Ligand Probes in Glucocorticoid-Resistant and -Sensitive Patients

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00600652
Enrollment
150
Registered
2008-01-25
Start date
2006-12-31
Completion date
Unknown
Last updated
2008-01-25

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

Conditions

Healthy

Keywords

glucocorticoid-receptor, flow cytometry, glucocorticoid-resistant, prediction

Brief summary

Monitoring the GR with a GR-MoAb and FITC-Dex probes by FCM would be useful and convenient in determination GR before the steroid treatment in clinical, especially in steroid resistant states, in order to design more efficient clinical treatment protocols.

Detailed description

In order to assess the efficacy of this method, 100 patients with nephrotic syndrome and systemic lupus erythematosus receiving sufficient prednisolone thereafter and 50 age- and sex-matched normal controls will be studied.

Interventions

None listed

Sponsors

Changhai Hospital
Lead SponsorOTHER

Study design

Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
15 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Clinical diagnosis of SLE and NS

Exclusion criteria

* Receiving hormone replacement therapy or had received hormone replacement therapy in three months before start of the study * Received drugs or drinks containing alcohol within one month * Having symptom such as infection * Supersensitivity and endocrine disturbance.

Outcome results

None listed

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