Fracture Clinical Trial
Official title:
Randomized Controlled Study Into Early Mobilization Following Internal Fixation of Isolated Ankle Fractures.
After a patient has fractured an ankle that then requires surgery, the recommendation is to remain in bed, with the operated leg elevated on pillows for 48 hours. This is a precautionary measure, as yet unsubstantiated by research, which is thought to minimize ankle swelling that can inhibit the healing of the surgical wound. However, prolonged bed rest can lead to other complications such as blood clots in the lungs or leg veins, or chest infections such as pneumonia. Prolonged bed rest is also known to cause weakness and a loss of fitness such that recovery may be slower. In this research the investigators will be randomly allocating patients to mobilize within 24 hours post operatively or to rest in bed for 48 hours with their leg well elevated. The investigators will measure length of stay and wound healing and integrity at 14 days. This study aims to investigate whether getting patients out of bed within 24 hours of surgery can accelerate recovery and reduce acute hospital length of stay without affecting wound healing. If bed rest for 2 days is not necessary, there will be benefits for the patient in terms of general health and ability, and for the hospital in terms of cost savings through shorter lengths of stay and patient through put. The investigators already know that early mobilization is beneficial following other types of orthopedic surgery such as hip fractures. This study aims to investigate if early mobilization following surgical management of ankle fractures is safe with specific regard to wound integrity and wound outcomes. This study will also investigate the effect of earlier mobilization on the length of time spent in the acute hospital and for those discharged directly home, the amount and type of support required. If early mobilization is found to be safe for wound healing and results in shorter in-hospital stays, this research will provide the confidence to endorse a change to current clinical practice.
n/a
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Caregiver), Primary Purpose: Treatment
Status | Clinical Trial | Phase | |
---|---|---|---|
Withdrawn |
NCT04470895 -
Impact of Drugs on the Risk of Falls in the Fracture Department of the Paris Saint-Joseph Hospital Group
|
||
Recruiting |
NCT02635022 -
Fragility Fracture Liaison Service and Anti-osteoporosis Medication Monitoring Service Study
|
||
Unknown status |
NCT02013986 -
Effects of Etomidate on Postoperative Circadian Rhythm Changes of Salivary Cortisol in Children
|
Phase 4 | |
Terminated |
NCT01248182 -
Bone to Skin Thickness Study: Obese Versus Normal Population
|
N/A | |
Recruiting |
NCT00969839 -
NovaLign Intramedullary Fixation System (IFS) for the Treatment of Humeral Fractures
|
Phase 4 | |
Completed |
NCT00520442 -
Acute Pediatric Fracture Analgesia Study
|
N/A | |
Completed |
NCT00115180 -
Racial and Ethnic Disparities in Acute Pain Control
|
N/A | |
Not yet recruiting |
NCT06402292 -
Surgical Treatment of Osteoarticular Infections Using Bioactive Bone Substitute
|
N/A | |
Recruiting |
NCT04947722 -
The PREVENT Trial: a Pragmatic Cluster Randomized Controlled Trial of a Multifaceted Fracture Prevention Model for Long-term Care
|
N/A | |
Recruiting |
NCT06107699 -
The CHARM Study-Coordinating Transitions From Hospital for Older Adults With Fractures
|
N/A | |
Completed |
NCT04532580 -
Clinical Validation of Boneview for FDA Submission
|
||
Completed |
NCT04237454 -
Thermal Imaging Compared to Skeletal Survey in Children Below 2 Years
|
N/A | |
Recruiting |
NCT05002335 -
Clinical and Radiological Outcomes of Medacta Shoulder System (BE)
|
||
Completed |
NCT02591043 -
Surgical Treatment of Low Energy Pelvic Fractures in the Elderly
|
N/A | |
Completed |
NCT02933359 -
Osteogenic Profiling of Normal Calvarial Bone
|
||
Completed |
NCT01049191 -
Bone Microarchitecture in Women With and Without Fracture
|
N/A | |
Completed |
NCT03431857 -
Multi Centre Study on TESS V2 Shoulder System
|
||
Recruiting |
NCT04133103 -
Early Mobilisation in the Surgical Robot Assisted Spinal Surgery
|
N/A | |
Completed |
NCT03993691 -
Wrist Fracture Evaluation With a Desktop Orthopedic Tomosynthesis System
|
N/A | |
Active, not recruiting |
NCT01719887 -
Effectiveness and Cost-effectiveness of Surgical Treatment of Humeral Shaft Fractures. Randomized Controlled Trial
|
N/A |