BMD: Bone Metastases Database of Patients Treated Surgically for Impending or Pathologic Fracture of Long Bones

Sponsor
Istituto Ortopedico Rizzoli (Other)
Overall Status
Recruiting
CT.gov ID
NCT03416959
Collaborator
(none)
120
1
108
1.1

Study Details

Study Description

Brief Summary

The aims of this study are to collect prospective data on the natural history of bone metastases (BMs) and skeleta related events (SREs),

Condition or Disease Intervention/Treatment Phase
  • Procedure: intramedullary fixation or endoprosthetic reconstruction

Detailed Description

The aims of this study are to evaluate clinical and biological factors of patients with BMs after reconstruction with intramedullary fixation (IMN) or endoprosthetic reconstruction (EPR) with a specific focus on (1) the rate of complication or failure; (2) differences in complication rates by anatomic site; (3) functional results as assessed by the Musculoskeletal Tumor Society System (MSTS); (4) differences in complication rate between patients treated with INM versus EPR; and (5) differences in survival in patients with metastatic bone disease based on disease-specific, laboratory, and demographic information.

Study Design

Study Type:
Observational
Anticipated Enrollment :
120 participants
Observational Model:
Case-Only
Time Perspective:
Prospective
Official Title:
Prospective Bone Metastases Database
Actual Study Start Date :
Jan 1, 2018
Anticipated Primary Completion Date :
Dec 31, 2026
Anticipated Study Completion Date :
Dec 31, 2026

Outcome Measures

Primary Outcome Measures

  1. Clinical outcomes after treatment of long bone metastases with intramedullary nail versus endoprosthetic reconstruction [24 months]

    The study includes the collection of clinical data (age, sex, Karnofsky score) and laboratory data related to the patient (erythrocyte sedimentation rate, C reactive protein, Alkaline phosphatase, white blood cells and hemoglobin) at the time of admission, data on the pathology (histotype, site of bone metastasis , presence of further skeletal or visceral metastases), type of surgery performed (stabilization versus resection).The objectives of this study is to examine clinical outcomes after after surgical treatment of bone metastases with a specific focus on differences in complication rate between patients treated with intramedullary nail versus endoprosthetic reconstruction

Secondary Outcome Measures

  1. Survival in patients undergoing surgery for metastatic bone disease [24 months]

    Provide a reliable and objective means of estimating survival in patients with metastatic bone disease based on disease-specific and laboratory tests

Other Outcome Measures

  1. Prognostic factor regarding erythrocyte sedimentation rate [24 months]

    erythrocyte sedimentation rate (mm/h)

  2. Prognostic factor regarding C reactive protein [24 months]

    C reactive protein (mg/dl)

  3. Prognostic factor regarding Alkaline phosphatase [24 months]

    Alkaline phosphatase (U/L)

  4. Prognostic factor regarding white blood cells [24 months]

    white blood cells (10/mm)

  5. Prognostic factor regarding hemoglobin [24 months]

    hemoglobin (g/dl)

  6. Prognostic factor regarding Karnofsky score [24 months]

    Karnofsky score (0/100)

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patients with long bone metastases treated surgically with intramedullary nail or endoprosthetic reconstruction
Exclusion Criteria:
  • Patients with bone metastases of the spine

Contacts and Locations

Locations

Site City State Country Postal Code
1 Istituto Ortopedico Rizzoli Bologna Italy 40136

Sponsors and Collaborators

  • Istituto Ortopedico Rizzoli

Investigators

  • Principal Investigator: Costantino Errani, MD, Istituto Ortopedico Rizzoli

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Costantino Errani, MD, PhD., Istituto Ortopedico Rizzoli
ClinicalTrials.gov Identifier:
NCT03416959
Other Study ID Numbers:
  • 0012807
First Posted:
Jan 31, 2018
Last Update Posted:
Mar 2, 2022
Last Verified:
Feb 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 2, 2022