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Safety of Immediate Weight-Bearing as Tolerated After Well-Reduced Geriatric Hip

Safety of Immediate Weight-Bearing as Tolerated After Well-Reduced Geriatric Hip Fracture

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06199739
Enrollment
14
Registered
2024-01-10
Start date
2020-01-01
Completion date
2023-05-05
Last updated
2024-01-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bony Weight Bearing Disorder

Keywords

fracture reduction, proximal femur fracture, geriatrics

Brief summary

Purpose: Proximal femur fracture is a major traumatic injury in elderly populations; however, practical postoperative weight-bearing protocols are lacking. Therefore, the purpose of the present study was to investigate whether early weight-bearing status after proximal femur nail fixation is associated with any loss of reduction and evaluate the clinical outcomes of this intervention. Patients and methods: For this prospective single center clinical trial study, we recruited 14 proximal femur fracture cases, classified by AO/OTA 2018, receiving intramedullary nail fixation. Clinical outcomes included the Harris functional hip score and VAS pain score. Additionally, demographic data, radiological parameters, time to weight-bearing, mortality rate, medical and surgical complications, and final ambulation status were recorded.

Interventions

The patients began early weight bearing under attending physician and physiotherapist surveillance within 48 hours after surgery. Patients were instructed to stand up near the bed, and muscle power, gait stability, and pain tolerance were recorded. The physiotherapist instructed the patients to perform early mobilization and weight bearing as tolerable by self-adjustment of body weight distribution over the bilateral lower extremities, and walking assistance was used to prevent repeat falling accidents.

Sponsors

Far Eastern Memorial Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

* Patients with AO/OTA type 31 fractures were included, and all fractures were classified using intraoperative fluoroscopy with traction on the fracture table.

Exclusion criteria

* Patients with pathological fractures, neurovascular insufficiency, ipsilateral lower extremity musculoskeletal injury, multiple fractures, or high risk of falling, including frequent falling accidents within 6 months, unsteady gait, ipsilateral neuropathy, limb weakness, and urinary incontinence were excluded.

Design outcomes

Primary

MeasureTime frameDescription
Harris Hip Functional scoreFunctional and radiographic evaluations was performed at months 1 postoperativelyThe questionaire to patient. (HHS score 0-100,\<60 poor,\>80 good)

Secondary

MeasureTime frameDescription
visual analog pain scoreRecord at months 1 postoperativelyIndependent assessor (VAS:0-10)
ComplicationFunctional and radiographic evaluations were performed at months 1, 3, 6, and 12 postoperativelyLoss of reduction, malunion or nonunion

Countries

Taiwan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026