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Determining Normal Range for Free Light Chains in Serum Among Twins

Not Applicable
Completed
Conditions
Multiple Myeloma
Interventions
Device: Free light chains
Registration Number
NCT04191057
Lead Sponsor
University of California, San Francisco
Brief Summary

The objective of this study is to recruit healthy adult identical and fraternal twins for the collection of one teaspoon of blood to be sent to the Clinical Lab at San Francisco General Hospital. The serum will be tested to determine the reference range for free light chains.

Detailed Description

Serum free light chains are used to assist in the diagnosis of multiple myeloma. The test measures kappa (K) and lambda (L) chains, and the calculation of the ratio of kappa to lambda (K/L). Previous studies have shown that the K/L ratio does not change over time (1 year). The hypothesis of this study is that healthy twins will have a K/L ratio that are close to each other in value, suggesting that this ratio is genetically linked.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
32
Inclusion Criteria
  • Healthy subjects 18-80 years.
  • Must be an identical or fraternal twin (both must be recruited)
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Exclusion Criteria
  • Symptoms suggestive of multiple myeloma (e.g., renal insufficiency, anemia, bone pain) -
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Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Healthy twinFree light chainsFree light chains of twins compared to non-twin siblings
Primary Outcome Measures
NameTimeMethod
Free light chain reference rangeOne month after the completion of the enrollment

Determination of the normal range for free light chains

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

San Francisco General Hospital

🇺🇸

San Francisco, California, United States

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