Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00859976
Other study ID # BMETEU.CR.EU27
Secondary ID UK REC Ref: 08/H
Status Completed
Phase N/A
First received
Last updated
Start date March 2009
Est. completion date May 2014

Study information

Verified date February 2019
Source Zimmer Biomet
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The randomised controlled trial will be carried out on patients that require a total hip replacement (THR) to reduce pain and restore their function. One way of fixing the hip joint to the bone is by coating the implant to encourage the body to grow bone onto the replacement hip. This study is aiming to find out whether the new (Bonemaster) coating allows increased bony growth onto the cup when compared to the usual (plasma-sprayed) coating. This may reduce the incidence of early failures due to poor bony attachment, which is a well known complication for early failure of total hip replacements.

The study will compare two different types of coating (BoneMaster and Plasma-sprayed) on the cup of the replacement hip. Density of the bone immediately surrounding the cup will be observed to see if there are differences between the two groups. The density of bone will be measured using standard x−ray assessment and in a smaller sample of 14 patients, using a special scan called Dual Energy X−ray Absorptiometry (DEXA Scan). Functional comparisons will be assessed through clinical scores.


Description:

The patients will be identified by the orthopaedic surgeon in the orthopaedic clinic and deemed suitable for the study if all inclusion and exclusion criteria are met. 210 patients will be recruited to the study and each patient will be randomised into either of the groups allowing 105 patients into each group. Patients will be followed up at 6 months, 1 year and 2 years after the surgery. All patients will have radiographic assessments at these follow-up intervals, as well as Harris Hip, Oxford Hip and Womac scores. This will allow comparison of the two groups.

The BoneMaster coating has been extensively tested in cell and animal studies and has been evaluated in one previous clinical study and showed favorable results. Further investigation is required to ensure the new coating may enhance bony growth allowing better fixation of the hips in the early period after the operation and also over a longer period of time. The growth needs to be measured using a more sensitive scan than radiographic assessment alone, called DEXA which was also used in the previous study.


Recruitment information / eligibility

Status Completed
Enrollment 167
Est. completion date May 2014
Est. primary completion date June 2012
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria

- Patients suitable for THR surgery with a diagnosis of Osteoarthritis

- Patients aged 40 -85 years old.

- Patients with limited co-morbidity - ASA I - III (low risk for surgery)

- Patients must be able to understand instructions and be willing to return for follow up

Exclusion Criteria

- Rheumatoid arthritis

- Patients requiring supplemental screw fixation

- Previous hip surgery to the affected hip

- Patients with significant co-morbidity - ASA IV - V (high risk for surgery)

- Dementia

- Neurological conditions affecting everyday functional ability and hip movement

- The patient is unable to give informed consent

- Patients who have suffered from cancer

- The patient is currently part of another research study

- Patients who need to take Non Steroidal Anti-inflammatory Drugs (NSAIDs) in the first 6 weeks after surgery

Study Design


Related Conditions & MeSH terms


Intervention

Device:
BoneMaster coated acetabular shell.
Bonemaster coated Exceed Acetabular Shell
Plasma Coated Acetabular Shell
Plasma HA coated Exceed Acetabular Shell

Locations

Country Name City State
United Kingdom William Harvey Hospital Ashford Kent

Sponsors (1)

Lead Sponsor Collaborator
Zimmer Biomet

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Record and Measure Bone Density Using DEXA Scans at 24 Months. DEXA scan cohort - DEXA scan was used to measure bone density. Below is the calculated net average bone mineral density (BMD) percentage change from baseline at 2 years. 2 years.
Primary Radiography to Determine Radiolucency in All Three DeLee & Charnley Zones of the Acetabulum. 34 patient cases without duplicated data were the basis for the radiographic analysis that was conducted: Bonemaster group, n = 12; Plasma-Sprayed group, n = 22. The degree of osseous-fixation was determined by grading: 1-2 mm radiolucencies, classed as not fixated; >2mm radiolucencies, classed as unstable. 2 years.
Secondary Secondary Outcomes Are Functional Assessment Using Harris Hip Score Modified Harris Hip Score, total score 0-100. A score of <70 is poor, 70-79 is fair, 80-89 is good, 90-100 is excellent. 2 years
Secondary Secondary Outcomes Are Clinical Assessment Using Oxford Hip Score Oxford Hip Score, scored 12-60. The Oxford hip score - this score was based on the original publication where each answer gives a score of 1-5. A score of 1 for each question, represented best outcome/least symptoms. Therefore a total score of 12 was the best overall outcome. 2 years.
Secondary Secondary Outcomes Are Clinical Assessment Using WOMAC Hip Score Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) Hip Score, Each question is scored on a scale of 0 (best health state) to 4 (worst health state); total WOMAC hip score, 0 being the best and 96 being the worst. 2 years
See also
  Status Clinical Trial Phase
Terminated NCT03940651 - Cardiac and Renal Biomarkers in Arthroplasty Surgery Phase 4
Recruiting NCT05649007 - Post-marketing Surveillance Study of the Saphir Stem in Primary Hip Surgery
Completed NCT04690647 - The Efficacy of Suprainguinal Fascia Iliaca Compartment Block for Analgesia After Elective Total Hip Replacement. N/A
Active, not recruiting NCT04322916 - Clinical Study With the RM Pressfit Vitamys Cup in Combination With a Mathys Stem
Completed NCT05399043 - Experience of Use and Biopsychosocial Effects of Robotic and Virtual Reality Devices in Neuromotor Rehabilitation N/A
Terminated NCT03185117 - Opioid Consumption After Hospital Discharge in Orthopedic Surgery
Recruiting NCT02884349 - The Relationship Between Component Position and RoM N/A
Completed NCT02404727 - Evaluation of Cemented and Cementless Fixation of Dual-mobility Hip Prosthesis in Elderly Patients With Osteoarthritis N/A
Completed NCT03282201 - A Survey on Blood Transfusions in Major Artrhoplasty Operations
Recruiting NCT05647629 - Observational Study of the Development of Low Back Pain After Total Hip Arthroplasty.
Recruiting NCT01135160 - Evaluation of Weight Bearing After Total Hip and Knee Replacement
Recruiting NCT06147401 - Comparison of PENG Associated With LFCN Block Versus FICB for Multimodal Analgesic Management in THA N/A
Not yet recruiting NCT06024161 - Weight Change and the Risk of Chronic Pain Following Hip and Knee Arthroplasties
Completed NCT01103882 - Short-Term Clinical Outcome of Total Hip Arthroplasty Using Larger Diameter of 4th Generation Ceramic Bearing
Not yet recruiting NCT06415825 - Preliminary Muscle Contraction in the Rehabilitation and Prevention of Degenerative Pain in the Locomotor System N/A
Completed NCT03219294 - Does Deep Neuromuscular Blockade Improve Operating Conditions During Total Hip Replacements? Phase 4
Completed NCT03834142 - NSS-2-BRIDGE Study for Total Knee and Hip Arthroplasties, Bariatric, and Kidney Transplant Surgeries N/A
Completed NCT04333264 - Clinical Analysis of Suction Drainage in Cementless Hip Replacement N/A
Completed NCT03875976 - Total Hip Arthroplasty: Fast Track Protocol is the Future? N/A
Completed NCT05470634 - Trail-running After Knee or Hip Arthroplasty