Porous Tantalum Rods Improve the Hip Joint Function of Patients With Avascular Necrosis of the Femoral Head
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|ClinicalTrials.gov Identifier: NCT02877472|
Recruitment Status : Unknown
Verified August 2016 by Heling Zhang, Qinghai University.
Recruitment status was: Recruiting
First Posted : August 24, 2016
Last Update Posted : August 24, 2016
|Condition or disease||Intervention/treatment||Phase|
|Femoral Neck Fracture||Device: porous tantalum rod Procedure: core decompression||Not Applicable|
History and current status of related studies: Femoral neck fracture can render the blood supply to the femoral head insufficient, leading to avascular necrosis of the femoral head. This often increases treatment difficulty and can have a strong influence on the recovery of hip joint function. Although core decompression for treatment of avascular necrosis of the femoral head has been largely used in clinical settings, the mid-term therapeutic effects are not satisfactory in some patients.
Biocompatibility is defined as the ability of a biomaterial, prosthesis, or medical device to perform with an appropriate host response. The biocompatibility of a bone implant and host influences the therapeutic effects. Therefore, biomaterials that are less likely to induce negative host responses may increase the therapeutic effects of such treatments for orthopedic diseases. A porous tantalum rod is a bone trabecula-like metal implant that is used to support weight-bearing areas of necrotic bone, preventing further collapse of the necrotic area. This implant has exhibited favorable effects in the early treatment of avascular necrosis of the femoral head. Although previous reports have focused on porous tantalum rod implantation for clinical treatment of avascular necrosis of the femoral head after fermoral neck fracture, few have assessed the long-term therapeutic effects or biocompatibility of porous tantalum rods.
Adverse events Possible adverse events include any expected or unexpected symptoms. If severe adverse events occur, information including the date of occurrence and measures taken related to the treatment of the adverse events will be reported to the principal investigator and the institutional review board within 24 hours.
Data collection, management, analysis, and open access Data collection: Case report forms with demographic data, disease diagnosis, accompanying diseases, drug allergy history, and adverse events will be collected , processed using Epidata software, collated, and then electrically recorded using a double-data entry strategy by data managers.
Data management: The locked electronic database will not be altered in any way, and will only be available to the project manager. Paper and electronic data regarding screening, informed consent, and clinical outcomes will be preserved at the Affiliated Hospital of Nantong University, China.
Data analysis: The electronic database will be made available to a professional statistician for statistical analysis. An outcome analysis report will be made by the statistician and submitted to the lead researchers. An independent data monitoring committee will supervise and manage the trial data with the goal of ensuring a scientific and stringent trial process, resulting in accurate and complete data.
Data open access: Anonymized trial data will be published at http://www.figshare.com.
Statistical analysis Statistical analysis will be performed by a statistician using SPSS 19.0 software and will follow the intention-to-treat principle. Normally distributed measurement data will be expressed as a mean, standard deviation, min, and max. Non-normally distributed measurement data will be expressed as a lower quartile (q1), median, and upper quartile (q3). McNemar's test will be used to compare the percentage of patients with excellent hip joint function as per Harris hip scores 12 months after surgery, the percentage of patients presenting with femoral head collapse, prosthesis loosening, peri-prosthesis infection, and incidence of complications 6 and 12 months after surgery. The Mann-Whitney U test will be used to compare the VAS score prior to and 1, 6, and 12 months after surgery. Statistical significance will be accepted when α = 0.05.
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||100 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||None (Open Label)|
|Official Title:||Porous Tantalum Rods Improve the Hip Joint Function of Patients With Avascular Necrosis of the Femoral Head After Femoral Neck Fracture Surgery: a Randomized Controlled Trial|
|Study Start Date :||May 2015|
|Estimated Primary Completion Date :||October 2016|
|Estimated Study Completion Date :||May 2017|
Experimental: Experimental group
Patients with avascular necrosis of the femoral head after femoral neck fracture surgery will undergo core decompression and porous tantalum rod implantation (experimental group).
Device: porous tantalum rod
Patients with avascular necrosis of the femoral head after femoral head fracture surgery receive treatment of core decompression and porous tantalum rod implantation
Other Name: Experimental group
Experimental: Control group
Patients with avascular necrosis of the femoral head after femoral neck fracture surgery will undergo core decompression (control group).
Procedure: core decompression
Patients with avascular necrosis of the femoral head after femoral head fracture surgery will undergo core decompression.
Other Name: Control group
- Harris hip scores [ Time Frame: 12 months after surgery ]To evaluate the recovery of hip joint function. The Harris hip score ranges from 0-100 points 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.
- Visual Analogue Scale (VAS) [ Time Frame: prior to and 1, 6, and 12 months after surgery ]To evaluate the severity of pain and ranges from 0-10, with higher scores indicating more severe pain.
- Incidences of complications [ Time Frame: 6 and 12 months after surgery ]To evaluate the safety of various implantation methods.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02877472
|Contact: Heling Zhang, Masteremail@example.com|
|Qinghai University Affiliated Hospital||Recruiting|
|Xining, Qinghai, China, 810001|
|Contact: Heling Zhang, Master 8613997262938 firstname.lastname@example.org|
|Principal Investigator:||Heling Zhang, Master||Affiliated Hospital of Qinghai University|