AzTrials
AzTrials

Femoral Neck FractureNCT02901938

Feasibility of Implantation of Cemented Femoral Stem for Osteoporotic Femoral Neck Fracture in Elderly Patients

A study testing cemented femoral stem and cannulated compression screws in people with Femoral Neck Fracture, run by Qinghai University.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
Search all trials

Trial summary

This study will investigate the effects of implantation of cemented femoral stem versus percutanous internal fixation with cannulated compression screws on hip joint function recovery, pains, femoral head collapse and sterile prosthesis loosening, peri-prosthesis infection, and the histocompatibility of prosthesis… Read more about this study

Who is it for?
Ages 60 to 80 years
Conditions the study is for
Femoral Neck Fracture
What is being tested?
cemented femoral stem and cannulated compression screws
Could I receive a placebo?
No, everyone receives an active treatment
How many people
100 participants
Where
No sites listed yet
Study dates
Jan 2016to Dec 2018
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 60 to 80 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Patients with avascular necrosis of the femoral head diagnosed according to the previous criteria: Bone nonunion as indicated by a clear fracture line on X-ray images 12 months after femoral neck fracture; cystic degeneration, sclerosis, and uneven density on X-ray images and CT scans
  • Patients with osteoporosis diagnosed according to a previous report: Bone density T value < -2.5 or bone mass decrease by 25%
  • Patients with femoral neck fracture diagnosed according to the previous criteria (Chen and Wang, 2013): Presence of a fracture line on anterior- posterior X-ray images of the hip joint, and CT and MRI examination in combination with clinical symptoms and physical sign are necessary if no fracture line appears
  • Age 60-80 years
  • Healthy and able to tolerate anesthesia and surgery
  • Provision of informed consent about participation and trial procedure

Who cannot join

  • Alcohol abuse or long-term use of hormone drugs
  • Infection of tissue around the hip joint
  • Bone metabolism disorders other than osteoporosis, such as renal osteodystrophy and osteomalacia
  • Heart, lung, brain, or other systemic diseases
  • Advanced malignant tumor
  • Recent cerebral hemorrhage, myocardial infarction, or failure of important organs
  • Injured limb with deep venous thrombosis
  • Inability to tolerate surgery

About this study

Official title: Feasibility of Implantation of Cemented Femoral Stem in the Treatment of Osteoporotic Femoral Neck Fracture in Elderly Patients: a Randomized Controlled Trial

This study will investigate the effects of implantation of cemented femoral stem versus percutanous internal fixation with cannulated compression screws on hip joint function recovery, pains, femoral head collapse and sterile prosthesis loosening, peri-prosthesis infection, and the histocompatibility of prosthesis material with host tissue in the elderly patients with osteoporotic fracture of proximal femoral neck complicated by avascular necrosis of the femoral head, which will provide scientific evidence for selecting surgical methods and internal fixation/artificial prosthesis material for osteoporotic fracture of proximal femoral neck in the elderly patients.

Read the detailed description

History and current related studies Femoral neck fracture is a common fracture that accounts for 3.58% of all fractures, easily occurs in the elderly with a gradually increased incidence, predisposes to bone nonunion, and greatly influences patient's mental and physical health. Bone nonunion easily occurs after femoral neck fracture because of anatomic position, biomechanical property and local blood supply. The objective of treatment of femoral neck fracture in patients aged 65 years and above is to rapidly restore lower limb function and reduce the complications caused by long term bed rest. Surgery for treatment of femoral neck fracture in the elderly is a satisfactory option because it not only contributes to recovery of joint function, but also decreases the incidence of complications. Several concerns are addressed during the process from design of internal fixation equipment to selection of clinical treatment protocol including minimizing surgical trauma, shortening length of surgery, and promoting functional recovery of hip joint. Osteoporosis is generally considered the most difficult problem to be solved after surgery for femoral neck fracture in the elderly patients. The key points of internal fixation for femoral neck fracture are to optimize bone space and strengthen fractured bone trabecula, yielding strong fixation biomechanically. Percutaneous internal fixation with cannulated compression screws has become a preferred treatment method of osteoporotic femoral neck fracture in elderly patients because of its short length of surgery and less blood loss, but insufficient holding power of used screws in the femoral neck cannot lead to strong fixation. Therefore, joint prosthesis is recommended for repair of femoral neck fracture in elderly patients. Implantation of femoral stem for treatment of early proximal femoral neck fracture has achieved confirmed clinical efficacy, but the long-term therapeutic effects in the treatment of osteoporotic fracture of proximal femoral neck remain poorly understood in patients with avascular necrosis of the femoral head.

Novelty of this study The investigators performed a search of PubMed, Web of Science and Wanfang Database up to August 2016 for articles regarding artificial prosthesis treatment of osteoporotic femoral neck fracture and found that the majority of previous reports focused on early femoral neck fracture and patients were generally followed up no more than 6 months. In this study, we will for the first time investigate the feasibility of implantation of cemented femoral stem versus percutaneous internal fixation with cannulated compression screws in the treatment of osteoporotic femoral neck fracture in the elderly patients with avascular necrosis of the femoral head necrosis through a 12 month follow up observation in terms of hip joint function, pain, histocompatibility of biomaterial with host tissue, and postoperative complications.

Data collection, management, analysis and open access An electronic data capture (EDC) system will be used for data collection and management. All study data will be in time recorded on the electronic case report form provided by the sponsor after patient's visits for recheck unless the outcomes cannot be achieved immediately. Thus, the recorded information can reflect patient's latest outcomes. Information accuracy will be rechecked after all included patients are followed up. The electronic data capture system will be locked by the project manager and will not be altered. All information relating to this trial will be preserved by Qinghai University Affiliated Hospital. The electronic data will be fully disclosed to a professional statistician for statistical analysis. Anonymized trial data will be published at http: www.figshare.com.

Statistical analysis Normally distributed continuous variables will be expressed as the mean ±SD and non-normally distributed variables will be expressed as median and quartile. Categorical variables will be expressed as counts and percentages. All data will be statistically analyzed using SPSS 19.0 software (IBM Corp., Armonk, NU, USA). Two-samples t-test or Mann-Whitney U test will be used for comparisons of Harris hip scores and VAS scores between percutaneous internal fixation with cannulated compression screws and implantation of femoral stem. The chi-square test or Fisher's exact test will be used for comparison of histocompatibility of biomaterial with host tissue. A level of P < 0.05 will be considered statistically significant.

Confidentiality Only the necessary data limited to studying the effectiveness and safety of percutaneous internal fixation with cannulated compression screws/implantation of femoral stem in the treatment of osteoporotic femoral neck fracture in the elderly patients will be collected and processed.

The privacy of information regarding the patients will be safeguarded during data collection and processing, and related laws and regulations should be abided by as follows:

  • The process of data collection is fair and legal.
  • The objective of data collection is specialized, identified and legal.
  • The collected data are abundant, relative but not excessive to the study objective, and the data unrelated to study objective will not be collected.
  • The collected data are accurate and will be updated if necessary.
  • Consent regarding data collection will be acquired before data collection.
  • The collected data will not be disclosed to any non-authorized persons or unlawfully mistaken, lost or altered. During the whole study period, the sponsor persons who have the rights to read the patient's information will not disclose the information.

Advantages and limitations of this study Advantages: This is a prospective, randomized controlled, open-label trial, in which we will evaluate the feasibility of percutaneous internal fixation with cannulated compression screws and implantation of cemented femoral stem in the treatment of osteoporotic femoral neck fracture complicated by avascular necrosis of the femoral head in the elderly patients through evaluating the safety and efficacy of these two surgical methods. In addition, scant information is reported on the biocompatibility of implants with host tissue in patients with osteoporotic femoral neck fracture in the elderly patients. Therefore, our findings will fill the gap.

Limitations: Quality of life and daily activities are also important indices used to evaluate the efficacy of surgery. But this study will be limited to human and material sources, so evaluations on but not limited to Short Form (36) Health Survey and Barthel Index of Activities of Daily Living will not be performed, which will be considered in future studies.

Being tested
cemented femoral stem, cannulated compression screws
Medical subject headings
Femoral Neck Fractures

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • cemented femoral stemProcedure or surgery

    The patients assigned even numbers will undergo implantation of cemented femoral stem.

  • cannulated compression screwsDevice

    The patients assigned even numbers will undergo percutaneous internal fixation with cannulated compression screws.

Study groups in NCT02901938
Study groupRoleWhat they receive
cemented femoral stem groupExperimentalThe patients with avascular necrosis of the femoral head complicated by osteoporotic femoral neck fracture will be randomly assigned to undergo implantation of cemented femoral stem.
Receives: Procedure: cemented femoral stem
cannulated compression screws groupExperimentalThe patients with avascular necrosis of the femoral head complicated by osteoporotic femoral neck fracture will be randomly assigned to undergo percutaneous internal fixation with cannulated compression screws.
Receives: Device: cannulated compression screws

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Changes of Harris hip scores

    To evaluate the recovery of hip joint function from the domains covering pain, function, absence of deformity, and range of motion, with higher scores indicating better hip joint function. Hip joint function is scored as follows: ≥ 90 is excellent, 80-89 very good, 70-79 good, and < 70 poor.

    Measured: at baseline, 1, 6 and 12 months after surgery

Secondary outcomes (1)
  1. Changes of VAS scores

    To evaluate the severity of pain and ranges from 0-10, with higher scores indicating more severe pain. A score of 0 represents no pain, scores > 0 and ≤ 3 represent mild pain, scores > 3 and ≤ 6 moderate pain, and scores > 6 and ≤ 10 severe pain.

    Measured: at baseline, 1, 6 and 12 months after surgery

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted15 Sep 2016 (estimated)
  2. Study startJan 2016
  3. Primary completionJun 2017 (estimated)
  4. Study completionDec 2018 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
100 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02901938
Sponsor's protocol ID
QinghaiUH_004
Status last verified
Sep 2016
First submitted
12 Sep 2016
Last updated
15 Sep 2016
Results posted
No
Data monitoring committee
Yes
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

A study testing cemented femoral stem and cannulated compression screws in people with Femoral Neck Fracture, run by Qinghai University.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 6 inclusion and 8 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 15 Sep 2016. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Changes of Harris hip scores (time frame: at baseline, 1, 6 and 12 months after surgery). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 15 Sep 2016; AzTrials last refreshed its copy on 8 Nov 2026.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in