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Sarcoma, Soft Tissue clinical trials

View clinical trials related to Sarcoma, Soft Tissue.

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NCT ID: NCT05813808 Completed - Sarcoma,Soft Tissue Clinical Trials

Low-dose Computer Tomography in Follow-up of Soft Tissue Sarcomas

Start date: June 1, 2017
Phase: N/A
Study type: Interventional

The goal of this interventional study is to compare sensitivity of regular chest x-ray to ultra-low-dose computed tomography to find pulmonary relapse in follow-up of soft tissue sarcoma. The main question[s] it aims to answer are: - Is ultra-low-dose computed tomography more sensitive than regular chest x-ray to find pulmonary relapse? - Does ultra-low-dose computed tomography detect the most fast-growing pulmonary metastases earlier than regular chest x-ray? Participants will have seven ultra-low-dose computed tomography imagings in addition to simultaneous routine protocol of chest x-rays. Participants therefore work as their own controls.

NCT ID: NCT04991883 Completed - Sarcoma,Soft Tissue Clinical Trials

Analysis of the Molecular Profile of the Mixofibrosarcoma of the Extremities

MFS
Start date: September 1, 2021
Phase:
Study type: Observational

Single institution case series review with a histological diagnosis of mixofibrosarcoma of the extremities from 01 Jan 1993 to 01 Dec 2017. The study will exam all the clinical, radiological, histological and immunohistochemical features of this tumour in all samples and in a limited serie of cases the presence of mutation of 50 genes cancer related.

NCT ID: NCT04347122 Completed - Sarcoma,Soft Tissue Clinical Trials

Tranexamic Acid in Radical Resection and Endoprosthetic Reconstruction

Start date: January 28, 2020
Phase: Phase 4
Study type: Interventional

This study intends to determine if any correlation exists between administration of TXA or not to musculoskeletal oncology patients undergoing endoprosthetic reconstruction and blood loss and blood transfusion rates.

NCT ID: NCT04248959 Completed - Osteosarcoma Clinical Trials

Prehabilitation to Improve Cancer Surgery Outcomes in AYA Patients With Extremity Sarcomas

PICaSO-ES
Start date: February 2, 2022
Phase: N/A
Study type: Interventional

The purpose of this study was to evaluate the feasibility of a multimodal prehabilitation intervention intended to optimize postoperative recovery in adolescents and young adults (AYAs) diagnosed with soft tissue and bone-based sarcomas of the upper and lower extremities (extremity sarcomas; ES).

NCT ID: NCT03798795 Completed - Clinical trials for Sarcoma, Soft Tissue

Radiomics for Tumor Grading of Soft Tissue Sarcomas.

Start date: October 1, 2017
Phase:
Study type: Observational

Radiomics is defined as a quantitative high-throughput analysis of imaging data combined with model development aiming to predict biological correlates or clinical endpoints. The investigators of this study hypothesize that radiomic features may correlate with pathology-defined tumor grading in soft tissue sarcoma patients. The aim of this study is to develop a predictive radiomics model for tumor grading determination.

NCT ID: NCT03058406 Completed - Clinical trials for Sarcoma, Soft Tissue

A Study on Safety and Efficacy in Patients With Soft Tissue Sarcomas

HAL03T
Start date: March 1, 2016
Phase:
Study type: Observational

The purpose of this study is to understand safety and efficacy in participants with soft tissue sarcomas.

NCT ID: NCT02994264 Completed - Sarcoma,Soft Tissue Clinical Trials

A Study to Compare Adjuvant Concurrent Chemoradiation (CCRT) to Adjuvant Radiation Therapy (RT) in Grade 2 and 3 Extremity Soft Tissue Sarcomas

Start date: August 2015
Phase: N/A
Study type: Observational

The aim of the study is to retrospectively evaluate the outcome of adjuvant concurrent chemoradiation delivered to patients with high grade non-metastatic soft tissue sarcomas of the extremities at the investigators institution paired with patients treated by adjuvant radiation therapy

NCT ID: NCT02897128 Completed - Clinical trials for Sarcoma, Soft Tissue

Transcutaneous Oxygen as a Predictor of Wound Healing Complications in Preoperatively Radiated Soft Tissue Sarcoma

Start date: July 2016
Phase:
Study type: Observational

Wound complications after sarcoma resection are frequent and potentially devastating problem. The burden of surgical wound complications in the lower extremity after preoperative external beam radiation therapy (EBRT) for soft tissue sarcoma is estimated at 43%. A noninvasive method of predicting complications would be extremely beneficial. The aim of this study is to evaluate the relationship between preoperative skin oxygenation and wound outcomes in a multi-center prospective analysis. This information could lead to a change in practice regarding surgical timing and adjunctive interventions to improve wound healing outcomes.

NCT ID: NCT02793050 Completed - Clinical trials for Sarcoma, Soft Tissue

Retrospective Study of Trabectedin in Soft Tissue Sarcomas

TrObs
Start date: June 15, 2016
Phase:
Study type: Observational

This is an independent, observational, retrospective post marketing study on the use of trabectedin in a clinical setting. A data collection on the clinical use of the drug will help to improve knowledge and might contribute to optimize the clinical use of the drug.

NCT ID: NCT02584309 Completed - Soft Tissue Sarcoma Clinical Trials

Doxorubicin With Upfront Dexrazoxane for the Treatment of Advanced or Metastatic Soft Tissue Sarcoma

Start date: February 22, 2016
Phase: Phase 2
Study type: Interventional

The purpose of this research study is to look at whether giving a drug called dexrazoxane with standard of care doxorubicin affects the progression of the disease. Dexrazoxane is often given at the same time as doxorubicin to help reduce the incidence and severity of disease of the heart muscle (which can be caused by doxorubicin). In January 2019 Eli Lilly and Company reported that the results of the Phase 3 study of olaratumab (Lartruvo), in combination with doxorubicin in patients with advanced or metastatic soft tissue sarcoma, did not confirm the clinical benefit of olaratumab in combination with doxorubicin as compared to doxorubicin alone. Therefore olaratumab is being removed from the front line standard of care regimen. Amendment #9 was made to the protocol to reflect these changes to the standard of care treatment.