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Soft Tissue Neoplasms clinical trials

View clinical trials related to Soft Tissue Neoplasms.

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NCT ID: NCT01276483 Completed - Clinical trials for Soft Tissue Neoplasms

Treatment Response Evaluation in Gastrointestinal Stromal Tumor (GIST) Patients

Start date: February 2011
Phase: N/A
Study type: Observational

The purpose of this study is to compare sensitivity, specificity and accuracy of PET, DW MRI and CT separately and combined for the evaluation of treatment response and progression-free survival in patients with GIST.

NCT ID: NCT01017978 Completed - Soft Tissue Tumors Clinical Trials

Quantitative MR Biomarkers for Sarcoma Treatment

Start date: July 2009
Phase: N/A
Study type: Interventional

To determine if MRI imaging can be used to accurately determine if a sarcoma is responding to the type of chemotherapy being used.

NCT ID: NCT00041886 Completed - Clinical trials for Soft Tissue Neoplasms

Radiofrequency Ablation of Painful Soft Tissue Neoplasms

Start date: July 2002
Phase: N/A
Study type: Observational

Radiofrequency ablation is used to treat patients with many different conditions. It is used to treat heart arrhythmia and benign bone tumors, and to control bleeding during surgery. It has been approved by the Food and Drug Administration for soft tissue ablation (removal). The technique involves inserting a probe, guided by computed tomography or ultrasound, and sending radio waves through the probe. The radio waves generate heat, which both destroys adjacent tissue and cauterizes blood vessels. This study will enroll 15 adults (age 18 or older) with soft tissue metastases who suffer pain that is not well controlled by other means, such as drugs. The goal is to reduce their pain or their use of analgesics by partially destroying some of their tumors. Patients will be ineligible for the study if they change the class of pain medication they use within 2 weeks before or 2 weeks after the study treatment. Patients will fill out short questionnaires about pain and daily activities (Brief Pain Inventory) before treatment and 1 day, 1 week, 1 month, 3 months, and 12 months after treatment to ascertain whether their pain is better controlled with less pain medication. For the treatment, most patients will receive local anesthetic in the area where the probe is inserted. Some patients may require general anesthesia. The probe will remain in place typically for 10 to 30 minutes. For larger tumors, it may be inserted at different positions.

NCT ID: NCT00001189 Completed - Neoplasms Clinical Trials

The Treatment of Grade I Sarcomas and Benign, Non-Metastasizing Highly Invasive Soft Tissue Tumors

Start date: December 1983
Phase: Phase 2
Study type: Interventional

Patients with Grade I soft tissue sarcomas or benign, non-metastasizing invasive soft tissue tumors will receive wide local excision and be prospectively randomized as to either receive or not receive radiation therapy.