Project JAY HAP Registration Study

Femoral Neck Fractures Clinical Trial

Official title:

A Prospective, Randomized, Multicenter Clinical Study in Elderly Chinese Subjects to Compare the Safety and Efficacy of the SS Bipolar Head and SL-TWIN Stem With Bipolar Head and SL-PLUS Stem in Hemiarthroplasty of the Hip

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02347397
• Other study ID #: 14-4561-01
• Status: Completed
• Phase: N/A
• First received: January 9, 2015
• Last updated: March 1, 2018
• Start date: April 29, 2015
• Est. completion date: October 16, 2017

Study information

• Verified date: March 2018
• Source: Smith & Nephew Orthopaedics (Beijing) Limited
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a prospective, randomized, multicenter clinical study in elderly Chinese subjects to compare the safety and efficacy of the SS Bipolar Head and SL-TWIN Stem with Bipolar Head and SL-PLUS Stem in hemiarthroplasty of the hip

Description:

Elderly patients, especially post-menopausal women, often suffer a femoral neck fracture due to osteoporosis, even with very little trauma. Femoral neck fracture is a common disease in elderly patients, it accounts for 3.6% of total body fractures. In China, as the population continues to age and life expectancy increases, the incidence of femoral neck fracture has significantly increased.

Hip replacement surgery includes total hip arthroplasty (THA) and hemiarthroplasty (HAP). Hemiarthroplasty of the hip involves replacement of the diseased, affected, or broken femoral head and/or neck with a prosthetic component. Hemiarthroplasty does not involve resurfacing of the acetabulum, and therefore a bipolar or unipolar prosthetic head articulates against the host acetabular articular cartilage. Avoiding the need, when appropriate, to resurface the acetabulum helps to minimize surgical trauma, operative time and dislocation risk, while preserving acetabular bone stock. These also result in shorter bed stay and faster recovery comparing with the THA.

There has been an increase in imported hip prostheses during the past decade, so that surgeons now have more choices of implants. However, the high cost of imported prostheses has become a barrier to the development of hip replacement in China and caused many patients requiring immediate hip replacement to have to delay or miss their surgery. The development and promotion of high-quality domestic joint implants and surgical instruments is the key to the development of joint replacement technique in China.

The primary objective of this study is to demonstrate non-inferiority of subjects implanted with the SS Bipolar Head + SL-TWIN Stem compared to a randomized concurrent control group of subjects implanted with the Bipolar Head + SL-PLUS Stem in terms of mean Harris Hip Score (HHS) at 1 year.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 134
• Est. completion date: October 16, 2017
• Est. primary completion date: October 16, 2017
• Accepts healthy volunteers: No
• Gender: All
• Age group: 65 Years to 90 Years

Eligibility

Inclusion Criteria:

• Male or female subjects, aged between 65 and 90 years inclusive of Chinese ethnicity.

• Subject presents with femoral neck fracture (Garden Type II, III, or IV) requiring hemiarthroplasty of the hip.

• Subject is able to move independently before the fracture, with or without the use of walking aids .

• Subject who is able to give voluntary, written informed consent to participate in the study and from whom consent has been obtained by signing and dating an EC-approved consent form.

• Subject who is able to understand this clinical study, co-operates with the investigational procedures and is willing to return to the hospital for all the required post-operative follow-ups for up to 12 months.

• Life expectancy of subject is over 2 years.

Exclusion Criteria:

• Bilateral hip disease with the anticipated need for bilateral hip implant during study participation (i.e., within the next 12 months).

• Subject experienced prior joint replacement surgery on any major joint (hip, knee) in lower limb within the last 12 months.

• Subject has known or suspected metal sensitivity.

• Subject is known to have insufficient bone stock resulting from conditions such as cancer, significant osteoporosis or metabolic bone disorders, which cannot provide adequate support and/or fixation to the prosthesis.

• Subject is severely obese (BMI>35).

• Subject is not suitable for hemiarthroplasty (i.e., inflammatory arthritis, pathological fractures, etc.)

• Subject had an active infection or sepsis (treated or untreated)

• Subject has conditions that may compromise implant stability or postoperative recovery (i.e., Paget's or Charcot's disease, vascular insufficiency, muscular atrophy, uncontrolled diabetes, moderate to severe renal insufficiency, hip abduction muscle strength less than grade IV or complete loss, or neuromuscular disease).

• Subject has an emotional or neurological condition that would affect their ability or willingness to participate in the study (e.g. cognitive disorder, mental illness, mental retardation).

• Subject is immunosuppressed, has an autoimmune disorder, or an immunosuppressive disorder. For examples, subject is on immunosuppressive therapy (corticosteroid hormones in large amounts, cytotoxic drugs, antilymphocytic serum or irradiation in large doses) or has acquired immunodeficiency syndrome (AIDS).

• Subject is known to be at risk for lost to follow-up, or failure to return for scheduled visits.

• Subject was enrolled in another investigational drug, biologic, or device study in the last 12 months.

• Known alcohol and/or drug abuse

Related Conditions & MeSH terms

• Femoral Neck Fractures

Intervention

Device:
• SS Bipolar Head + SL-TWIN Stem
Subject will undergo hemiarthroplasty surgery with SS Bipolar Head & SL-TWIN Stem
• Bipolar Head + SL-PLUS Stem
Subject will undergo hemiarthroplasty surgery with Bipolar Head & SL-PLUS Stem

Locations

Country	Name	City	State
China	Inner Mongolia Bao Gang Hospital	Baotou	Inner Mongolia
China	Haikou People's Hospital	Haikou	Hainan
China	Luoyang Orthopedic-Traumatological Hospital	Luoyang	Henan
China	The First Teaching Hospital of Xinjiang Medical University	Ürümqi	Xinjiang
China	Traditional Chinese Medicine Hospital of Xinjiang Uygur Autonomous Region	Ürümqi	Xinjiang

Sponsors (1)

Lead Sponsor	Collaborator
Smith & Nephew Orthopaedics (Beijing) Limited

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Barthel Index		1 year post-operative
Other	SF-12 Health Survey		1 year post-operative
Other	Number of adverse events		Up to 1 year post-operative
Primary	Harris Hip Score		1 year post-operative
Secondary	Composite Clinical Success, as indicated by A) No revision of any device component; and B) Total Harris Hip Score greater than or equal to 80 (excellent to good score); and C) Radiologic success.	A successful individual outcome for a subject in hemiarthroplasty will be characterized at 1 year postoperative by a composite of three success criteria: A. No revision of any device component; and B. Total Harris Hip Score greater than or equal to 80 (excellent to good score); and C. Radiologic success.	1 year post-operative