Ireland
--:--IST
Recruiting Observational

Assessing the Clinical Effectiveness of Serum Biomarkers in the Diagnosis of Metastatic Uveal Melanoma

NCT01438658 · tracked via the Priya Life Science Israel tracker
Phase
Observational
Started
2011-09
Last updated
2011-09-28

Condition(s) studied

Uveal Melanoma

Study summary

Uveal melanoma is the most common primary intraocular tumor in adults. The local treatment is effective, but patients still die of metastatic disease. It has been shown that early diagnosis of a few isolated metastases can result in a clean surgical excision of the metastases and an extension of the expected survival from 7-12 months to over 10 years on some patients.

Many serum biomarkers are employed in Oncology. It makes sense to try the relevant ones in the diagnosis of metastatic uveal melanoma.

The investigators hypothesis is that a soluble serum biomarker level changes upon development of metastatic disease either by secretion by the tumor cells themselves or by their environment. Detection of changes in biomarker level may lead to the diagnosis of metastases before they can be detected by imaging modalities, thus allowing for early treatment of the metastases and a better chance of success.

Eligibility

Sex
ALL
Min age
—
Max age
—
Healthy volunteers
No
Inclusion Criteria: * diagnosis of uveal melanoma Exclusion Criteria: * refusal to participate in the study

Primary outcome measure(s)

  • Significant increase in biomarker level that could be linked with detection of metastases by imaging — up to 12 months before diagnosis of metastases
    Serum will be taken on every clinic visit from the day of diagnosis and on. Change in biomarker level will be assessed from one visit to the previous one, and correlated with imaging information on detection of metastases.

Trial sites (1)

FacilityCityRegionStatus
Specialized Ocular Oncology Service, Hadassah-Hebrew-University Medical Center Jerusalem Israel Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT01438658 on ClinicalTrials.gov ↗ ← All trials in Israel