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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02984215
Other study ID # 69HCL16_0720
Secondary ID
Status Completed
Phase N/A
First received October 31, 2016
Last updated December 2, 2016
Start date January 1990
Est. completion date June 2016

Study information

Verified date October 2016
Source Hospices Civils de Lyon
Contact n/a
Is FDA regulated No
Health authority France: The Commission nationale de l’informatique et des libertés
Study type Observational

Clinical Trial Summary

Plasma-cell post-transplantation lymphoproliferative disorders (PC-PTLD) are rare monomorphic PTLD divided into plasma cell myeloma (PCM) and plasmacytoma-like lesion (PLL) PTLD. To date, there is no exhaustive published cytogenetic data on PC-PTLD. The investigators report array-based comparative genomic hybridization (aCGH) of 10 cases of PCM and PLL-PTLD.


Recruitment information / eligibility

Status Completed
Enrollment 10
Est. completion date June 2016
Est. primary completion date January 2012
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- WHO classification 2008 as monomorphic PCM (plasma cell myeloma) or PLL (plasmacytoma like lesion) / PTLD (post transplantation lymphoproliferative disorders).

Exclusion Criteria:

- Other than PCM or PLL PTLD at diagnosis

Study Design

Time Perspective: Retrospective


Related Conditions & MeSH terms


Locations

Country Name City State
France Centre hospitalier Lyon sud Pierre Bénite Rhône Alpes

Sponsors (1)

Lead Sponsor Collaborator
Hospices Civils de Lyon

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Genome wide array-based comparative genomic hybridization (aCGH) At diagnosis of PTLD, Day 0. No
Secondary Overall survival according to aCGH complexity Overall survival (OS) was calculated from date of diagnosis to date of death from any cause, up to 130 months. No