Clinical Trials Logo

Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05825456
Other study ID # AnkaraUniOrtho
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date January 1, 2022
Est. completion date January 1, 2025

Study information

Verified date April 2023
Source Ankara University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This is a single center prospective study to compare the short term results of prosthesis, nail and plate-screw surgeries for metastatic pathologic fractures.


Description:

The most common bone tumor in elderly is metastatic bone tumors. With the prolonged life expectancy in cancer patients, the management of the metastases became an essential topic. Pathological fractures should be examined and managed with a different perspective. They usually cannot be healed by conservative methods and require surgical intervention. The primary goals of surgical intervention are to relieve pain and mobilize the patient as soon as possible. The aim of the study is to compare the short-term functional endoprosthetic recontruction, intramedullary nailing and open reduction internal fixation. The primary tumor of the patient, applied chemotherapy and radiotherapy, Mirel risk score, Charlson comorbidity index, and PathFx 3.0 survival will be evaluated preoperatively. The type of the operation will be decided at the multidisciplinary tumor council of ankara University.


Recruitment information / eligibility

Status Recruiting
Enrollment 200
Est. completion date January 1, 2025
Est. primary completion date January 1, 2024
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - metastatic pathologic fracture - operated via endoprosthesis, intramedullary nail or plate & screws Exclusion Criteria: - primary bone tumor - conservative management - neuromuscular disease - periprosthetic fractures - less than 1 month follow up

Study Design


Intervention

Procedure:
endoprosthetic reconstruction
This is a type of surgery in which the affected part of the bone and joint is removed, and replaced by a prosthesis.
Intramedullary nailing
This is a type of surgery in which the affected bone is stabilized by a nail. The affected part could be removed or retained. If removed, the defect is filled with bone cement.
Open reduction internal fixation with plate and screws
This is a type of surgery in which the affected part of the bone is visualized completely, after the reduction is achieved, the fixation is provided with appropriate plates and screws. Again the affected part could be removed or retained. If removed, the defect is filled with bone cement.

Locations

Country Name City State
Turkey Ankara University Medical Faculty Ankara Altindag

Sponsors (1)

Lead Sponsor Collaborator
Ankara University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Musculoskeletal Tumor Society (MSTS) score MSTS score is for evaluating the patients with bone tumors. It consists of six domains; scored on a 0 to 5 scale and transformed into an overall score ranging from 0 to 100% with a higher score indicating better function. Preoperative
Primary Musculoskeletal Tumor Society (MSTS) score MSTS score is for evaluating the patients with bone tumors. It consists of six domains; scored on a 0 to 5 scale and transformed into an overall score ranging from 0 to 100% with a higher score indicating better function. Postoperative 1st day
Primary Musculoskeletal Tumor Society (MSTS) score MSTS score is for evaluating the patients with bone tumors. It consists of six domains; scored on a 0 to 5 scale and transformed into an overall score ranging from 0 to 100% with a higher score indicating better function. Postoperative 1st week
Primary Musculoskeletal Tumor Society (MSTS) score MSTS score is for evaluating the patients with bone tumors. It consists of six domains; scored on a 0 to 5 scale and transformed into an overall score ranging from 0 to 100% with a higher score indicating better function. Postoperative 1st month
Primary Toronto Extremity Salvage Score (TESS) TESS is widely used for the functional assessment of patients following surgery for musculoskeletal tumours. In the TESS system, specific movements for independent living and functionality are questioned and scored.While the worst score is 0, the best score for the lower extremity is 150, and the best score for the upper extremity is 145. Preoperative
Primary Toronto Extremity Salvage Score (TESS) TESS is widely used for the functional assessment of patients following surgery for musculoskeletal tumours. In the TESS system, specific movements for independent living and functionality are questioned and scored.While the worst score is 0, the best score for the lower extremity is 150, and the best score for the upper extremity is 145. Postoperative 1st day
Primary Toronto Extremity Salvage Score (TESS) TESS is widely used for the functional assessment of patients following surgery for musculoskeletal tumours. In the TESS system, specific movements for independent living and functionality are questioned and scored.While the worst score is 0, the best score for the lower extremity is 150, and the best score for the upper extremity is 145. Postoperative 1st week
Primary Toronto Extremity Salvage Score (TESS) TESS is widely used for the functional assessment of patients following surgery for musculoskeletal tumours. In the TESS system, specific movements for independent living and functionality are questioned and scored.While the worst score is 0, the best score for the lower extremity is 150, and the best score for the upper extremity is 145. Postoperative 1st month
Primary Visual analog scale (VAS) VAS is a widely used scale for pain. 0 means no pain where 10 means unbearable pain. Preoperative
Primary Visual analog scale (VAS) VAS is a widely used scale for pain. 0 means no pain where 10 means unbearable pain. Postoperative 1st day
Primary Visual analog scale (VAS) VAS is a widely used scale for pain. 0 means no pain where 10 means unbearable pain. Postoperative 1st week
Primary Visual analog scale (VAS) VAS is a widely used scale for pain. 0 means no pain where 10 means unbearable pain. Postoperative 1st month
Primary Upper Extremity Functional Scale (UEFS) UEFS is a functional scale for upper extremity. It is not specific for tumor patients. Preoperative
Primary Upper Extremity Functional Scale (UEFS) UEFS is a functional scale for upper extremity. It is not specific for tumor patients. Postoperative 1st day
Primary Upper Extremity Functional Scale (UEFS) UEFS is a functional scale for upper extremity. It is not specific for tumor patients. Postoperative 1st week
Primary Upper Extremity Functional Scale (UEFS) UEFS is a functional scale for upper extremity. It is not specific for tumor patients. Postoperative 1st month
Primary Disabilities of Arm, Shoulder and Hand (DASH) DASH is a widely used functional scale for upper extremity. It is not specific for tumor patients. Preoperative
Primary Disabilities of Arm, Shoulder and Hand (DASH) DASH is a widely used functional scale for upper extremity. It is not specific for tumor patients. Postoperative 1st day
Primary Disabilities of Arm, Shoulder and Hand (DASH) DASH is a widely used functional scale for upper extremity. It is not specific for tumor patients. Postoperative 1st week
Primary Disabilities of Arm, Shoulder and Hand (DASH) DASH is a widely used functional scale for upper extremity. It is not specific for tumor patients. Postoperative 1st month
Primary Lower Extremity Functional Scale (LEFS) LEFS is a functional scale for lower extremity. It is not specific for tumor patients. Preoperative
Primary Lower Extremity Functional Scale (LEFS) LEFS is a functional scale for lower extremity. It is not specific for tumor patients. Postoperative 1st day
Primary Lower Extremity Functional Scale (LEFS) LEFS is a functional scale for lower extremity. It is not specific for tumor patients. Postoperative 1st week
Primary Lower Extremity Functional Scale (LEFS) LEFS is a functional scale for lower extremity. It is not specific for tumor patients. Postoperative 1st month
Primary Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) WOMAC is a widely used functional scale for lower extremity. It is not specific for tumor patients. Preoperative
Primary Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) WOMAC is a widely used functional scale for lower extremity. It is not specific for tumor patients. Postoperative 1st day
Primary Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) WOMAC is a widely used functional scale for lower extremity. It is not specific for tumor patients. Postoperative 1st week
Primary Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) WOMAC is a widely used functional scale for lower extremity. It is not specific for tumor patients. Postoperative 1st month
Secondary Days at hospital after surgery Hospitalization length required after the surgery. up to 1 month
Secondary Survival Time that the patient lives after the surgery up to 3 months
See also
  Status Clinical Trial Phase
Recruiting NCT05094804 - A Study of OR2805, a Monoclonal Antibody Targeting CD163, Alone and in Combination With Anticancer Agents Phase 1/Phase 2
Enrolling by invitation NCT00068003 - Harvesting Cells for Experimental Cancer Treatments
Recruiting NCT05798611 - Study of ART0380 in Patients With Biologically Selected Solid Tumors Phase 2
Not yet recruiting NCT04931420 - Study Comparing Standard of Care Chemotherapy With/ Without Sequential Cytoreductive Surgery for Patients With Metastatic Foregut Cancer and Undetectable Circulating Tumor-Deoxyribose Nucleic Acid Levels Phase 2
Recruiting NCT05566574 - A Study of RP-3500 in Combination With Standard Radiation Therapy in People With Solid Tumor Cancer Phase 1/Phase 2
Recruiting NCT05036681 - A Phase II Study of Futibatinib and Pembrolizumab in Metastatic Microsatellite Stable Endometrial Carcinoma Phase 2
Withdrawn NCT00005030 - SCH 66336 Before Surgery in Treating Patients With Colorectal Cancer That Has Metastasized to the Liver Phase 1
Recruiting NCT05525858 - KPMNG Study of MOlecular Profiling Guided Therapy Based on Genomic Alterations in Advanced Solid Tumors II
Recruiting NCT04085029 - Role of Ablative Radiotherapy in the Management of Metastatic Disease: A Patient Data Registry
Recruiting NCT06058988 - Trastuzumab Deruxtecan (T-DXd) for People With Brain Cancer Phase 2
Not yet recruiting NCT05981170 - Rurality Adapted Physical Activity Sport Health
Not yet recruiting NCT03058809 - Evaluation of Viatarâ„¢ Oncopheresis System in Removing CTC From Whole Blood Phase 1/Phase 2
Completed NCT02529553 - A Study of LY3076226 in Participants With Advanced or Metastatic Cancer Phase 1
Terminated NCT01929941 - An Open-Label Study of a Novel JAK-inhibitor, INCB047986, Given in Patients With Advanced Malignancies Phase 1
Completed NCT01302808 - Romidepsin and Erlotinib Hydrochloride in Treating Patients With Stage III or Stage IV Non-Small Cell Lung Cancer Phase 1
Terminated NCT00918645 - Calcium-41 (41Ca) Chloride Aqueous Solution in Diagnosing Patients With Prostate Cancer and Bone Metastasis N/A
Completed NCT00795678 - Chemotherapeutic Agents in Brain/Breast N/A
Withdrawn NCT00769990 - Genistein in Treating Patients Undergoing External-Beam Radiation Therapy for Bone Metastases Phase 1/Phase 2
Completed NCT00557102 - Cetuximab and Combination Chemotherapy as First-Line Therapy in Treating Patients With Colorectal Cancer That Has Spread to the Liver and/or Lung Phase 2
Recruiting NCT00398437 - Magnetic Resonance Imaging for the Early Detection of CNS Metastases in Women With Stage IV Breast Cancer N/A