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Bone Cancer clinical trials

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NCT ID: NCT04650594 Terminated - Knee Disease Clinical Trials

Functional Outcomes of Knee Protheses for Malignant Tumours of Bone

ISOMUTAR
Start date: July 1, 2021
Phase: N/A
Study type: Interventional

The placement of mega knee prosthesis is a necessity after a large tumor resection and oncological. These mega knee prostheses implanted in the context of oncological surgery have been very few evaluated in the literature. Active knee extension is essential in order to walk properly. The study propose the evaluation of this prosthesis by checking the possibility of locking of the prosthetic joint and thus the possibility of active walking. A more in-depth, isokinetic analysis at 1 year of follow-up will also be done in an exploratory manner, as the literature has no data on this subject.

NCT ID: NCT03525392 Terminated - Colorectal Cancer Clinical Trials

Study to Evaluate the Safety and Activity (Including Distribution) of 177Lu-3BP-227 in Subjects With Solid Tumours Expressing Neurotensin Receptor Type 1.

Start date: May 3, 2018
Phase: Phase 1
Study type: Interventional

This study was conducted to advance new treatment for patients with metastatic or locally advanced cancers expressing Neurotensin receptor 1 (NTSR1). This study was the first time the investigational drug called 177Lu-3BP-227 was administered to patients under controlled conditions of a clinical study. The purpose of this study was to evaluate how safe the investigational drug is as well to verify how well it is tolerated by patients after several intravenous administrations. In addition, the effect of the study drug on tumoral lesions and how it distributes throughout the body and at which rate it is removed from the body was evaluated. Since 177Lu-3BP-227 is a radio-labelled drug, it also measured how the emitted radiation is distributed throughout the body (dosimetry). The study consisted of a phase I dose escalation part. The study originally planned to include a phase II study however due to early termination (not due to safety concerns) the study did not progress to phase II and was stopped during phase I. For the phase I dose escalation part, it was anticipated that approximately 30 subjects will be included, in up to six escalation steps. No expansion cohorts were implemented.

NCT ID: NCT02443103 Terminated - Metastasis Clinical Trials

Study Evaluating the Biologic Activity of Guanabenz in Bone Metastasis

Start date: May 7, 2015
Phase: N/A
Study type: Interventional

This study will explore the biologic activity of guanabenz in reducing bone turn over in solid tumor patients with bone metastasis. If successful, this repurposing of an already, generic drug could benefit patients faster than manufacturing a novel expensive compound.

NCT ID: NCT01541358 Terminated - Bone Cancer Clinical Trials

Sodium Fluoride PET/CT for the Evaluation of Skeletal Cancer

Start date: May 2012
Phase: N/A
Study type: Interventional

This clinical trial studies fluorine F-18 sodium fluoride positron emission tomography (PET)/computed tomography (CT) in diagnosing bone tumors in patients with cancer. Diagnostic procedures, such as fluorine F-18 sodium fluoride PET/CT, may help find and diagnose bone cancer

NCT ID: NCT01313884 Terminated - Bone Cancer Clinical Trials

Cyclophosphamide, Doxorubicin, Vincristine w/ Irinotecan and Temozolomide in Ewings Sarcoma

Start date: May 2011
Phase: Phase 2
Study type: Interventional

The outcome of patients with metastatic Ewings Sarcoma is poor with current standard of care chemotherapy, with less than 30% survival. Based on recent encouraging pediatric literature we have designed this trial to improve the outcome of patients with metastatic Ewings sarcoma using Irinotecan and Temozolomide in addition to standard chemotherapy.

NCT ID: NCT01163539 Terminated - Bone Cancer Clinical Trials

Cyberknife Radiosurgery and Quality of Life

Start date: July 2010
Phase: N/A
Study type: Observational

The purpose of this study is to look at pain control and QOL improvement after treatment with CK Radiosurgery for spinal metastases.

NCT ID: NCT00960063 Terminated - Neoplasms Clinical Trials

A Study of Robatumumab (SCH 717454, MK-7454) in Combination With Different Treatment Regimens in Pediatric Participants With Advanced Solid Tumors (P05883, MK-7454-006)

Start date: November 11, 2009
Phase: Phase 1
Study type: Interventional

This is a Phase 1/1B, non-randomized, open-label, dose-escalation study of robatumumab (SCH 717454, MK-7454) administered in combination with chemotherapy in pediatric participants with solid tumors, to be conducted in conformance with Good Clinical Practices. This study will evaluate the safety, tolerability and dose-finding of robatumumab when administered in combination with temozolomide and irinotecan (Arm A); or cyclophosphamide, doxorubicin, and vincristine (Arm B), or ifosfamide and etoposide (Arm C). The primary study hypothesis is that robatumumab can be safely administered in combination with chemotherapy regimens in pediatric participants with solid tumors.

NCT ID: NCT00632294 Terminated - Bone Cancer Clinical Trials

Retrospective Study of the Biomechanical Properties of Large Allografts

Start date: December 2007
Phase: N/A
Study type: Observational

Primary Objectives: 1. To evaluate the material properties, histomorphometric indices, bone mineral density (BMD), and presence of microfractures in retrieved large allograft cortical bone specimens removed from orthopaedic oncology patients. 2. To correlate physical properties to patient demographics and medical treatment received.

NCT ID: NCT00127387 Terminated - Prostate Cancer Clinical Trials

Enbrel Versus Placebo With Radiation Therapy to Combat Fatigue and Cachexia

Start date: May 2001
Phase: Phase 2/Phase 3
Study type: Interventional

Patients who receive radiation therapy often have fatigue or a decrease in feeling well causing a "wasting" away. For patients with advanced disease of lung cancer, prostate cancer, or cancer that has spread to the bone, it is hoped that this drug may decrease this. If patients feel better during treatments they can complete the therapy without any breaks in treatment. For treatment to be most effective, it should be given in the amount needed, on a particular schedule.