Active clinical trials for "Bone Marrow Diseases"

This is a multicenter，randomized, double-blind, active-controlled, parallel-group study comparing efficacy and safety of LY01011 (recombinant anti-RANKL human monoclonal antibody injection) and Xgeva® in patients with bone metastases from solid tumors.

This study will give comparison of the bone pain remission and the adverse reaction of Zoledronic acid combine with High dose fractionation radiotherapy(30Gy/10f) and Zoledronic acid combine with low dose fractionation radiotherapy(15Gy/5f) . The purpose of this trial is to prove whether Zoledronic acid combine radiotherapy can reduce radiotherapy dose in treatment of non-small cell lung cancer bone metastasis'pain relief or not.

The clinical trial is a stage 3 study to determine the role of fentanyl transmucosal in the prevention of pain induced by mobilization in patients receiving a bone metastasis radiation for bone metastasis irradiations

A phase1 study to demonstrate [68Ga]P15-041 binding to bone metastases in prostate cancer and determination of human dosimetry.

Evaluate the feasibility of single cell sequencing technology based on three-dimensional bionic capture network; To build a risk prediction model of bone related events based on single cell sequencing; To verify the risk prediction model of bone related events by single cell sequencing; To verify the comprehensive treatment of non-small cell lung cancer ( NSCLC) bone metastases.

This phase 0 trial studies whole body fluorine F 18 sodium fluoride positron emission tomography (PET)/computed tomography (CT) scan and whole body magnetic resonance imaging (MRI) in finding bone metastases in patients with prostate cancer. Diagnostic procedures, such as whole body fluorine F 18 sodium fluoride PET/CT scan and whole body MRI, may help find and diagnose bone metastases.

Hypothesis: Radiosensitization using Xeloda should improve the rate of complete pain relief. Primary Objective: To determine the frequency of pain relief for the proposed regimen. Secondary Objective(s): To determine the duration of pain relief and narcotic relief for the proposed regimen. To determine the frequency of narcotic relief for the proposed regimen. To determine the toxicity of concurrent UFT and radiotherapy in patients with bone metastases.

Investigators performed a prospective randomized controlled trial for comparing postoperative clinical and radiological outcomes between C3 laminectomy with laminoplasty and C3-6 laminoplasty.

Prospective, monocentric, comparative, non randomised Primary objective : - to compare the diagnostic accuracy of sodium fluoride PET-CT and MRI using the conventional block and diffusion sequence in the search for bone metastases Secondary objectives : compare accuracy of MRI diffusion and conventional MRI explore the evolution of the results of the different types of imaging over time or under treatment for patients with repeated examinations at 6 months

Model of this study is a combined both retrospective chart review and follow up survey. Data of 4 hospitals will be used to find out the efficacy of conservative treatment in cervical myelopathy.