Effect of Denosumab on Inflammatory Osteolytic Lesion Activity in Total Hip Arthroplasty

NCT ID: NCT01358669

Last Updated: 2022-08-29

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 24 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2011-12-14
• Study Completion Date: 2021-12-31

Brief Summary

Although hip replacement surgery is a successful way of dealing with the pain and immobility caused by hip arthritis, 10% of the hip replacements carried out in the UK fail within 10 years. The main reason for this is the development periprosthetic osteolysis, that is, loss of bone around the site of the hip replacement. The osteolysis is thought to be due to the small particles of debris worn from the surfaces of the hip implant. These particles cause a reaction in the blood cells around the joint which in turn affects bone cells and leads to a loss of bone around the implant. The joint implant will then eventually become loose and unstable, a condition known as aseptic loosening. At present the only way to treat aseptic loosening is to have another operation to secure the hip joint, known as revision surgery. Revision surgery is not always successful and exposes the patient to the risk of major surgery.

In this study we explore the potential for giving a medication (denosumab) that may prevent the loss of bone around the hip replacement implant. We will recruit patients who have been listed for revision surgery. One group of patients will be given a single dose of denosumab; another group will be given a placebo (dummy drug). At the time of the revision surgery a small sample of the bone from around the hip replacement will be taken and examined under the microscope. Comparisons will be made between the patients having the denosumab and those having placebo to find out whether the denosumab is having a beneficial effect on the bone surfaces. If successful, this study will lead to further studies to develop the use of denosumab to prevent aseptic loosening.

Detailed Description

This is a single centre, double blinded, randomized, controlled trial of denosumab compared to placebo in adults undergoing revision surgery of total hip arthroplasty due to prosthesis related osteolysis. A total of 30 subjects will be enrolled into the study. Subjects will be randomized to receive either denosumab or placebo. 15 participants will be assigned to each treatment arm.

1. 60mg denosumab by injection as a single dose

2. Placebo by injection as a single dose After they have given informed consent, all participants will have a screening visit (Visit 1). Participants who are eligible after completing all screening assessments will be randomly assigned to receive one of the two treatments. All screening procedures will be completed within 14 (±7) days before beginning the medication. Study medication will be given at visit 2, which will occur 8 weeks (56 ±7 days) before the date of the planned revision surgery. Participants will attend for 5 visits in total as shown below. Visit 1, Baseline, 2 weeks (±7 days)before being given the study medication

• Informed consent
• Personal and demographic data
• Medical history
• Physical exam
• Weight and height
• Concomitant medication (other medications being taken at the visit)
• Blood samples for eligibility, and bone turnover markers
• Urine samples for bone turnover markers
• Vital signs including blood pressure (BP), heart rate (HR) and temperature
• Personal and demographic data
• Medical history
• Physical exam
• Weight and height
• Concomitant medication (other medications being taken at the visit)
• Blood samples for eligibility, and bone turnover markers
• Urine samples for bone turnover markers
• Vital signs including blood pressure (BP), heart rate (HR) and temperature Visit 2, Randomization and administration of denosumab or placebo (day 0)
• Blood sampling for bone turnover markers
• Urine sampling for bone turnover markers
• Changes to medical history
• Changes to concomitant medications
• Record of adverse events
• Oxford and Harris hip scores (by questionnaire)
• Pregnancy test if applicable
• Administration of medication
• Vital signs including BP, HR and temperature
• Conebeam CT scan of the affected hip Visit 3, Week 4 (±7 days)
• Blood sampling for bone turnover markers
• Urine sampling for bone turnover markers
• Changes to medical history
• Record of adverse events
• Record of concomitant medications
• Oxford and Harris hip scores
• Vital signs including BP,HR and temperature
• Check on injection site Visit 4, Week 8 (±14 days) (Revision Surgery)
• Standard preoperative admission procedures
• Blood sampling for bone turnover markers
• Urine sampling for bone turnover markers
• Changes to medical history
• Adverse events recorded
• Record of concomitant medications
• Oxford and Harris hip scores
• Bone and tissue biopsy
• Vital signs including BP, heart rate and temperature Visit 5, Week 14 (±7 days) (Safety follow up visit)
• Blood sampling for bone turnover markers
• Urine sampling for bone turnover markers
• Changes to medical history
• Adverse events recorded
• Record of concomitant medications
• Oxford and Harris hip score
• Vital signs including BP and heart rate
• Pregnancy test if applicable
• Plain Xray of the pelvis and hip

Conditions

Revision Surgery of Total Hip Arthroplasty

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: DOUBLE

Study Groups

Denosumab

In this study we explore the potential for giving a medication (denosumab) that may prevent the loss of bone around the hip replacement implant

Group Type: ACTIVE_COMPARATOR

Denosumab

Intervention Type: DRUG

60mg denosumab by injection as a single dose

Placebo

Placebo

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: OTHER

Placebo by injection as a single dose

Interventions

Denosumab

60mg denosumab by injection as a single dose

Intervention Type: DRUG

Placebo

Placebo by injection as a single dose

Intervention Type: OTHER

Other Intervention Names

Prolia

Eligibility Criteria

Inclusion Criteria

• Participants must be men or women over 30 years of age undergoing revision THA surgery for periprosthetic osteolysis / aseptic loosening affecting the pelvis and / or femur.
• Participants must also be willing and able to give fully informed consent.
• Participants must have osteolysis / aseptic loosening affecting fully cementless, hybrid, or fully cemented THA prosthesis

Exclusion Criteria

• Known prosthesis infection
• Pregnancy / Breast feeding
• Oral bisphosphonate therapy (current use, previous use within the last 12 months, previous 3 or more years cumulative use)
• Administration of intravenous bisphosphonate, fluoride or strontium within the last 5 years
• Participation in ongoing or previous denosumab clinical trials
• Administration of any of the following treatments within the last 12 months
• TH or PTH derivatives, eg, teriparatide
• anabolic steroids or testosterone
• glucocorticosteroids (> 5 mg prednisone equivalent per day for more than 10 days)
• systemic hormone replacement therapy
• selective estrogen receptor modulators (SERMs), eg, raloxifene tibolone, calcitonin or calcitriol
• Any subject in whom denosumab is contraindicated according to the local SmPC of denosumab (SC 60 mg every 6 months in UK)
• Current hypocalcemia (albumin adjusted serum calcium below 2.13 mmol/L)
• History of rheumatoid arthritis
• History of Paget's disease
• Malignancy (except basal cell carcinoma, cervical or breast ductal carcinoma in situ) within the last 5 years
• Renal insufficiency assessed by eGFR <30
• Known sensitivity to mammalian cell derived drug products
• Any organic or psychiatric disorder, or laboratory abnormality which, in the opinion of the Investigator, will prevent the subject from completing the study or interfere with the interpretation of the study results
• Any disorder that, in the opinion of the Investigator, may compromise the ability of the subject to give written informed consent and/or comply with study procedures
• Evidence of alcohol or substance abuse within the last 12 months that the Investigator believes would interfere with understanding or completing the study
• Subject is currently enrolled in or has not yet completed at least 30 days since ending other investigational device or drug trial(s), or subject is receiving other investigational agent(s).

• Minimum Eligible Age: 30 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Amgen

INDUSTRY

Sponsor Role: collaborator

University of Sheffield

OTHER

Sponsor Role: collaborator

Sheffield Teaching Hospitals NHS Foundation Trust

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

J M Wilkinson, PhD, FRCS (Tr&Orth)

Role: PRINCIPAL_INVESTIGATOR

Sheffield Teaching Hospitals NHS Foundation Trust/University of Sheffield

Locations

Academic Unit of Bone Metabolism

Sheffield, South Yorkshire, United Kingdom

Countries

United Kingdom

Other Identifiers

STH15714

Identifier Type: -

Identifier Source: org_study_id