Geriatrisk distal femur
Enkelt implantat versus dobbelt implantat-fiksering af ekstraartikulære og komplette artikulære lårbensfrakturer hos ældre patienter
The goal of this clinical trial is to compare two types of surgical fixation in patients with specific kinds of distal femur fractures. The main questions it aims to answer is which operation for distal femur fractures is better for efficient return to work and everyday activities.
Studieoversigt
Status
Status
Betingelser
Betingelser
Intervention / Behandling
Intervention / Behandling
Detaljeret beskrivelse
Fractures of the distal femur are severe and common injuries sustained by older adults. Despite advances in implant technology, these injuries continue to have an unacceptably high rate of nonunion (failure to heal) of approximately 20%. This adverse outcome requires additional surgery to achieve fracture healing, which prolongs recovery and further delays return to activities of daily living and impacts quality of life. Despite numerous studies of a variety of different surgical treatment strategies, the incidence of nonunion remains high. Therefore, any novel strategy to reduce the risk of nonunion and accelerate return to activities after distal femur fracture warrants rigorous study. The goal of this study is to investigate a potential treatment for distal femur fractures that has the potential to improve the likelihood of fracture healing and accelerate return of patient function during the healing process.
Undersøgelsestype
Undersøgelsestype
Tilmelding (Anslået)
Tilmelding
Fase
Fase
- Ikke anvendelig
Kontakter og lokationer
Studiekontakt
Studiekontakt
- Navn: Laurence Kempton, M.D.
- Telefonnummer: 7042553035
- E-mail: laurence.kempton@advocatehealth.org
Studiesteder
-
-
North Carolina
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Charlotte, North Carolina, Forenede Stater, 28204
- Rekruttering
- Atrium Health
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-
Deltagelseskriterier
Berettigelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
Inclusion Criteria:
- Age greater than or equal to 55 years
- Surgically treated displaced distal femur extra articular or complete articular fractures
Exclusion Criteria:
- Patients with injury features that preclude treatment with 2 implants
- Patients unlikely to follow-up due to homelessness, or planning follow up at another institution
- Body Mass Index (BMI) > 40
- Injury due to ground level fall
- Patient that speaks neither English or Spanish
- Patients with multisystem injuries that could preclude return to work
- < 55 years of age
- Prisoner
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Ingen (Åben etiket)
Antal våben
Våben og indgreb
Deltagergruppe / ArmDeltagergruppe / Arm |
Intervention / BehandlingIntervention / Behandling |
|---|---|
|
Andet: Single Implant Fixation
Single implant fixation with either a precontoured lateral locking plate or an intramedullary nail which is the current standard of care. |
Lateral precontoured 4.5 mm distal femur plate or an intramedullary nail at the surgeon's discretion. Standard-of-care techniques will be used by the surgeon for fracture reduction and implant placement. |
|
Andet: Dual Implant Fixation
Dual implant fixation with either a lateral locking plate plus an intramedullary nail or a lateral locking plate plus a supplemental medial plate which is the current standard of care. |
Lateral precontoured distal femur plate and either (1) an intramedullary nail or (2) a medial plate. The medial plate must span the extra-articular portion of the fracture and must have stiffness of a 3.5 mm reconstruction plate, 3.5 mm limited contact dynamic compression plate, or greater. |
Hvad måler undersøgelsen?
Primære resultatmål
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Number of Unions
Tidsramme: 6-week, 3, 6, 12 months
|
Union, as determined by the treating surgeon, will be assessed via radiographs and documented as a dichotomous outcome (yes/no), and time to union will also be captured. Nonunion will be captured via surgeon diagnosis or return to the operating room for nonunion treatment. |
6-week, 3, 6, 12 months
|
|
Total Surgical Time - Reoperations
Tidsramme: 6-week, 3, 6, 12 months
|
The total surgical time during any reoperations will be collected from the medical record. |
6-week, 3, 6, 12 months
|
|
Number of Reoperations
Tidsramme: 6-week, 3, 6, 12 months
|
Details regarding reoperations will also be collected, whether or not the operation results in an inpatient admission. |
6-week, 3, 6, 12 months
|
Sekundære resultatmål
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Number of Resource Utilizations
Tidsramme: 6-week, 3, 6, 12 month
|
Healthcare utilization, including all hospitalizations, emergency department visits, clinic visits, imaging, and physical therapy sessions after the index stay following injury will be documented at all follow-up visits. |
6-week, 3, 6, 12 month
|
|
Return to Work - International Physical Activity Questionnaire (IPAQ) Scores
Tidsramme: Week 6
|
Completion of the International Physical Activity Questionnaire (IPAQ). The IPAQ is a validated, self-report measure that captures detailed information about participation in a wide range of physical activities, including the number of days and amount of time spent in the previous 7 days. Responses for each type of physical activity are then transformed into the number of Metabolic Equivalent for Tasks (METs), and a METs/week is calculated for each patient. To get a continuous variable score from the IPAQ (MET minutes a week) it is considered walking to be 3.3 METS, moderate physical activity to be 4 METS and vigorous physical activity to be 8 METS. Higher scores meaning more activity. |
Week 6
|
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Return to Work - International Physical Activity Questionnaire (IPAQ) Scores
Tidsramme: Month 3
|
Completion of the International Physical Activity Questionnaire (IPAQ). The IPAQ is a validated, self-report measure that captures detailed information about participation in a wide range of physical activities, including the number of days and amount of time spent in the previous 7 days. Responses for each type of physical activity are then transformed into the number of Metabolic Equivalent for Tasks (METs), and a METs/week is calculated for each patient. To get a continuous variable score from the IPAQ (MET minutes a week) it is considered walking to be 3.3 METS, moderate physical activity to be 4 METS and vigorous physical activity to be 8 METS. Higher scores meaning more activity. |
Month 3
|
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Return to Work - International Physical Activity Questionnaire (IPAQ) Scores
Tidsramme: Month 6
|
Completion of the International Physical Activity Questionnaire (IPAQ). The IPAQ is a validated, self-report measure that captures detailed information about participation in a wide range of physical activities, including the number of days and amount of time spent in the previous 7 days. Responses for each type of physical activity are then transformed into the number of Metabolic Equivalent for Tasks (METs), and a METs/week is calculated for each patient. To get a continuous variable score from the IPAQ (MET minutes a week) it is considered walking to be 3.3 METS, moderate physical activity to be 4 METS and vigorous physical activity to be 8 METS. Higher scores meaning more activity. |
Month 6
|
|
Return to Work - International Physical Activity Questionnaire (IPAQ) Scores
Tidsramme: Month 12
|
Completion of the International Physical Activity Questionnaire (IPAQ). The IPAQ is a validated, self-report measure that captures detailed information about participation in a wide range of physical activities, including the number of days and amount of time spent in the previous 7 days. Responses for each type of physical activity are then transformed into the number of Metabolic Equivalent for Tasks (METs), and a METs/week is calculated for each patient. To get a continuous variable score from the IPAQ (MET minutes a week) it is considered walking to be 3.3 METS, moderate physical activity to be 4 METS and vigorous physical activity to be 8 METS. Higher scores meaning more activity. |
Month 12
|
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Time to Walking Without an Assistive Device
Tidsramme: 6-week, 3, 6, 12 months
|
Use of an assistive device will be abstracted from the medical record and/or collected via patient interview at each follow up time point. |
6-week, 3, 6, 12 months
|
|
Prescribed Weight Bearing Status
Tidsramme: 6-week, 3, 6, 12 months
|
The prescribed weightbearing status will be captured from discharge instructions and clinic notes. |
6-week, 3, 6, 12 months
|
|
Fear of Movement -Tampa Scale for Kinesiophobia (TSK) Scores
Tidsramme: 6-week, 3, 6, 12 months
|
Tampa Scale for Kinesiophobia (TSK) will be utilized to measure fear of movement. This scale is 17 items and uses a 4-point Likert scale ranging from 'strongly disagree' to 'strongly agree'. The TSK is a validated measure for surgical and musculoskeletal patients. The 17 item TSK total scores range from 17 to 68 where the lowest 17 means no or negligible kinesiophobia, and the higher scores indicate an increasing degree of kinesiophobia. |
6-week, 3, 6, 12 months
|
|
Health Related Quality of Life - Patient-Reported Outcomes Measurement Information System (PROMIS) Scores
Tidsramme: 6-week, 3, 6, 12 months
|
The PROMIS-29 includes seven domains: depression, anxiety, physical function, pain interference, fatigue, sleep disturbance, and ability to participate in social roles and activities. A 5-point Likert scale is used for each question and norm-based total scores (range 0-100) have been calculated so that 50 represents the mean and one standard deviation is 10 points. Higher scores represent better function. |
6-week, 3, 6, 12 months
|
|
Global Health Status - Veterans RAND 12 Item Health Survey (VR12) Scores
Tidsramme: 6-week, 3, 6, 12 months
|
The VR-12 is a measure of global health that corresponds to seven domains: general health, physical functioning, role limitations, pain, fatigue, social functioning, and mental health. Scores range from 0 to 100. 0 indicates the lowest level of health and 100 indicates the highest level of health. |
6-week, 3, 6, 12 months
|
|
Work Productivity and Activity Impairment Questionnaire Scores
Tidsramme: 6-week, 3, 6, 12 months
|
The Work Productivity and Activity Impairment Questionnaire (WPAI) questionnaire is an instrument to measure impairments in both paid work and unpaid work. It measures absenteeism, presenteeism as well as the impairments in unpaid activity because of health problem during the past seven days. WPAI outcomes are expressed as impairment percentages, with higher numbers indicating greater impairment and less productivity. |
6-week, 3, 6, 12 months
|
|
Numeric Pain Rating
Tidsramme: 6-week, 3, 6, 12 months
|
Patients will be asked to rate their current pain on a visual analog scale. In a Numerical Rating Scale (NRS), patients are asked to circle the number between 0 and 10, 0 and 20 or 0 and 100 that fits best to their pain intensity. Zero usually represents 'no pain at all' whereas the upper limit represents 'the worst pain ever possible'. |
6-week, 3, 6, 12 months
|
|
Pain Inventory (BPI)
Tidsramme: 6-week, 3, 6, 12 months
|
Pain will be assessed using the Brief Pain Inventory (BPI). The BPI is a commonly used and validated 15-item measure of pain intensity and interference with daily life. The BPI measures how much pain has interfered with seven daily activities, including general activity, walking, work, mood, enjoyment of life, relations with others, and sleep. BPI pain interference is typically scored as the mean of the seven interference items. Pain Score: 1 - 4 = Mild Pain. Worst Pain Score: 5 - 6 = Moderate Pain. Worst Pain Score: 7 - 10 = Severe Pain. Higher scores meaning higher pain. |
6-week, 3, 6, 12 months
|
|
Patient-Reported Outcomes Measurement Information System (PROMIS)-29 Subscale--Pain Interference
Tidsramme: 6-week, 3, 6, 12 months
|
The PROMIS-29 scales will be scored using a T-score metric method. A score of 50 points represents the population average for each scale, and 10 points represent one standard deviation - scores (range 0-100). Higher scores means a higher level of pain interference. |
6-week, 3, 6, 12 months
|
|
Presence of Post-Traumatic Arthritis (PTOA) - Kellgren Lawrence (KL) Classification
Tidsramme: 1 year
|
If PTOA is present, Kellgren Lawrence (KL) classification will be assessed by the panel of reviewers and documented. Higher scores represent worse PTOA. Grade 0 - Normal articular cartilage. Grade I - Softening and swelling. Grade II - Fragmentation and fissuring of less than 0.5 inches. Grade III - Fragmentation and fissuring of greater than 0.5 inches. Grade IV - Erosion down to the subchondral bone. |
1 year
|
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Presence of Post-Traumatic Arthritis (PTOA) - Paley Grading System (PGS)
Tidsramme: 1 year
|
If PTOA is present, the Paley Grading System (PGS) will be assessed by the panel of reviewers and documented. Higher scores represent worse PTOA. Standard joint space with no evidence of degeneration was set as Grade 0. Normal joint space with the occurrence of osteophytes, subchondral sclerosis, and cysts was set as Grade 1. Joint space narrowing was set as Grade 2. Disappeared joint space was set as Grade 3. |
1 year
|
|
Geriatric Depression Scale
Tidsramme: 6-week, 3, 6, 12 months
|
This scale has been validated in many studies and is unique in that it is tailored to a geriatric population by distinguishing between undiagnosed dementia and depression. Patients will also complete this scale to measure depression as part of health-related quality of life. The Geriatric Depression Scale (GDS) includes a total score range of 0 to 15. A score of 5 or more suggests depression. A score of 6 on this scale has a 94% sensitivity and 85% specificity for Diagnostic and Statistical Manual of Mental Disorders (DSM) diagnosed depression. |
6-week, 3, 6, 12 months
|
|
Morphine Milligram Equivalents (MME)
Tidsramme: 6-week, 3, 6, 12 months
|
To evaluate pain medication as a confounder to pain scores and complications MME will be calculated at each time point. To assess MME as a confounder, MME will be compared by treatment group at each time point. |
6-week, 3, 6, 12 months
|
|
Total Surgical Time - Index Surgery
Tidsramme: Baseline
|
The total surgical time during the index surgery will be collected from the medical record |
Baseline
|
|
Total Hospital Days
Tidsramme: Baseline, 6-week, 3, 6, 12 months
|
Total hospital days, including the index hospitalization and any subsequent inpatient stays will be captured |
Baseline, 6-week, 3, 6, 12 months
|
Samarbejdspartnere og efterforskere
Sponsor
Sponsor
Efterforskere
Efterforskere
- Ledende efterforsker: Laurence Kempton, M.D., Wake Forest University Health Sciences
Datoer for undersøgelser
Studer store datoer
Studiestart (Faktiske)
Studiestart
Primær færdiggørelse (Anslået)
Primær færdiggørelse
Studieafslutning (Anslået)
Studieafslutning
Datoer for studieregistrering
Først indsendt
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Først opslået
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering sendt
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
Andre undersøgelses-id-numre
- IRB00139405
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
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