Calcium Absorption in Patients With Rothmund-Thomson Syndrome
Completed · Not applicable
Conditions studied: Rothmund-Thomson Syndrome
In brief
Osteosarcoma is the most common malignant bone tumor in children and adolescents. Because cure rates for osteosarcoma have remained stagnant for the past several decades despite numerous trials of chemotherapy agents, novel therapies based on the understanding of the molecular pathogenesis of osteosarcoma are needed. Rothmund-Thomson Syndrome (RTS) is a genetic disorder affecting many parts of the body and resulting in major skeletal abnormalities. This disease also has the propensity to increase the risk of developing cancer, particularly osteosarcoma. Two-thirds of RTS patients have a high risk of developing osteosarcoma. Therefore, it is important to understand the impact of RTS on the skeletal phenotype (as measured by bone density) in order to develop effective therapies to battle osteosarcoma.
Key facts
- Study ID
- NCT01304407
- Run by
- Baylor College of Medicine
- People needed
- 29
- Starts
- 2011-03-01
- Expected to finish
- 2017-02-01
- Last updated by the study team
- 2020-07-23
Who can join
Age: 4 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patients at least four years of age who have been diagnosed clinically with RTS by a physician.
You may not qualify if…
- Any person who does not meet the inclusion criteria.
Where it is running
- Baylor College of Medicine / Texas Children's Hospital — Houston, Texas, United States
Full record on ClinicalTrials.gov
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