Lymphoma in the Orbit
1 other identifier
observational
50
1 country
1
Brief Summary
Imaging techniques have considerably improved over the last decades and ocular adnexal lymphomas (OALs) nowadays can be detected. As major advances in immunophenotyping and molecular diagnostics in histology have been achieved offering an accurate diagnosis, the investigators would like to introduce that surgical biopsy of an orbital lymphoma becomes crucial for the possibility of a correct diagnosis and proper treatment. As radiotherapy accomplished great preciseness as well and OALs respond excellently to radiation, this therapy should be the treatment of choice in local defined lymphomas instead of blind treatment with steroids. Radiation results in great local control rates of 85% to 100%
- Trial with surgical intervention
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Feb 2011
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 1, 2011
CompletedFirst Submitted
Initial submission to the registry
February 23, 2011
CompletedFirst Posted
Study publicly available on registry
February 24, 2011
CompletedStudy Completion
Last participant's last visit for all outcomes
May 1, 2012
CompletedNovember 4, 2011
November 1, 2011
February 23, 2011
November 3, 2011
Conditions
Keywords
Interventions
Patients after biopsy of orbital lymphoma
Eligibility Criteria
Patient, who underwent biopsy of an ocular adnexal lymphoma between 01/2006 and 12/2010 at the University Hospital Zurich, Division of Ophthalmology
You may qualify if:
- \>17 years of age
- underwent biopsy of an ocular adnexal lymphoma between 01/2006 and 12/2010 at the University Hospital Zurich, Division of Ophthalmology
- diagnosis histologically proven
You may not qualify if:
- less than 18 years of age
- patient underwent no MRI before surgery (biopsy)
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University Hospital Zurich, Ophthalmic Clinic
Zurich, Canton of Zurich, 8091, Switzerland
Study Officials
- PRINCIPAL INVESTIGATOR
Karla Chaloupka, MD
University Hospital Zurich, Ophtalmic Clinic
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
February 23, 2011
First Posted
February 24, 2011
Study Start
February 1, 2011
Study Completion
May 1, 2012
Last Updated
November 4, 2011
Record last verified: 2011-11