Fracture Femur

4

Review clinical trials related to Fracture Femur. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Cognitive and Physical Recovery After Hip Fracture in Frail Patients Using Digital Rehabilitation Technology

The aim of this study is to evaluate whether integrating a technology-based rehabilitation approach with conventional therapies in the rehabilitation of patients with proximal femoral fracture may be advantageous compared with conventional therapy alone. Specifically, the objective is to assess whether the addition of technology-assisted rehabilitation can improve cognitive function, in addition to motor function and overall abilities, compared with conventional rehabilitation alone. Furthermore, the study intends to explore the feasibility of implementing technology-assisted rehabilitation as a stable and routine component of everyday clinical practice, also considering the perspective of healthcare professionals.

Participants needed: 30
Trial details
Age: 65-89Biological sex: AllType: InterventionalSponsor: C.O.T. Cure Ortopediche Traumatologiche S.p.A.Updated: Mar 13, 2026Locations: 2
Eligibility criteria

Age between 65 and 89 years [+4]

Age > 90 years [+9]

Status: Recruiting

Feasibility of Integrating Local Vibration Into Rehabilitation of Elderly Patients After Hip Fracture

Fractures of the upper end of the femur in elderly patients are the 2nd most common fracture. A fracture leads to a syndrome of psychomotor maladjustment, encouraged by pain and aggravated by hospitalisation. In 2014, 50,000 women and 16,000 men suffered this type of fracture every year. The consequences are serious, with a one-year mortality rate of 20 to 24% and an institutionalisation rate of 25%. In 2015, the direct cost of hip fracture in France was estimated at around €1 billion. In line with the recommendations of the National Institute for Health and Care Excellence (NICE) and the results of meta-analyses, it is recommended that, in the absence of surgical or medical contraindications, patients should be assessed within 24 hours of hip fracture surgery, with a view to initiating early mobilisation and multidisciplinary rehabilitation. It has been shown in healthy subjects that prolonged application of localised vibrations optimises nerve capacity, leading to an increase in maximum voluntary force. For population of frail elderly post-operative patients, this localised vibration technique could accelerate and improve functional recovery, particularly in terms of muscle strength, joint mobility and pain. A reduction in muscle loss is hoped for, with benefits in terms of tolerance compared with neurostimulation. As part of the implementation of the above-mentioned recommendations, the investigators wish to assess the quality of the integration of this technique, already in use in the department on an ad hoc basis, into the organisation of the department and of the patient's care pathway as a complement to the rehabilitation protocols, by identifying the obstacles and facilitating factors. The study will also provide the first estimates of the effect on muscle recovery. The investigator hypothesise that this local vibration protocol can be integrated into the rehabilitation department's work schedule and into the patient's care pathway, and that it will be acceptable to both the patient and the nursing staff.

Participants needed: 25
Trial details
Age: 75+Biological sex: AllType: InterventionalSponsor: Hospices Civils de LyonUpdated: Feb 9, 2026Locations: 1
Eligibility criteria

Patients aged 75 or over who have undergone surgery for a fracture of the upper... [+4]

Persons deprived of their liberty by a judicial or administrative decision [+7]

Status: Recruiting

Oral Supplementation With a Formulation Based on Cetylated Fatty Acids for Post-fracture Long Bone Healing

This clinical study aims to evaluate the potential benefits of a formulation based on Cetylated Fatty Acids in improving fracture healing of long bones in the lower limbs. The investigational product is administered orally over a 12-week period. Study procedures are limited to standard imaging techniques (radiography and echography), blood sampling, and completion of validated quality of life questionnaires.

Participants needed: 100
Trial details
Age: 18-85Biological sex: AllType: InterventionalSponsor: Pharmanutra S.p.a.Updated: Dec 23, 2025Locations: 6
Eligibility criteria

Between 18 and 85 years old [+6]

Treatment with vitamin D for medical purpose (Non-union, osteoporosis…) [+22]

Status: Recruiting

Single Shot Exparel vs Catheters in Lower Extremity Trauma

This study will compare the use of single-shot Exparel, a long-acting local anesthestic, with the use of catheters that deliver a continuous flow of the short-acting local anesthetic ropivacaine. The comparison will be done in patients who receive preoperative adductor and sciatic nerve blocks prior to orthopedic surgery for traumatic lower extremity injury. The patients' pain will then be monitored for up to 72 hours after injection, measuring every 12 hours after injection until the 72-hour mark. Opioid consumption (measured in morphine milligram equivalents) will also be tracked over this time period.

Participants needed: 90
Trial details
Phase: Phase 4Age: 18+Biological sex: AllType: InterventionalSponsor: George Washington UniversityUpdated: Oct 28, 2025Locations: 1
Eligibility criteria

Closed lower extremity orthopedic injury [+2]

Allergy to local anesthetics [+7]