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Hip Fractures clinical trials

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NCT ID: NCT03300219 Recruiting - Hip Fractures Clinical Trials

Tele-rehabilitation Intervention for People Post Hip Fracture - Pilot Study

Start date: January 1, 2017
Phase: N/A
Study type: Interventional

Most surviving hip-fracture patients experience reduced mobility and lose their functional ability, which increases the risk of complications and rehospitalization. Post-discharge transitional programs to reduce readmissions have shown some success. Telerehabilitation refers to the use of technologies to provide rehabilitation services to people in their homes. Considering the need for long-term follow-up care for people with hip fracture, in-home telerehabilitation could increase independence, decrease hospital stays and reduce the burden for caregivers. The purpose of the pilot study is to examine the feasibility and acceptability of the research methods evaluating telerehabilitation with adults who have experienced hip fracture, in preparation for a larger randomized controlled study. A one-group (N=6) pre-test/post-test design is currently being constructed. Results of the pilot study will be used to determine what adaptations to the design may be required to ensure successful implementation. Recruitment, retention and attendance rates, as well as percentages completing the outcome measures, will be examined to plan the time frame of the main trial. The intervention will include 10 videoconferencing sessions from an occupational therapist in the presence of the primary caregiver. Each session will be utilized to guide the participants to achieve their self-identified goals, focusing on problem-solving for daily life situations and on the ability to implement the discussed strategies for a variety of activities.

NCT ID: NCT03298425 Completed - Fractures, Closed Clinical Trials

The Use of NMES With Pelvic Fracture Rehabilitation

Start date: February 2015
Phase: N/A
Study type: Interventional

The purpose of the study is to investigate if using an electrical stimulation machine to see if it can help strengthen the muscles around the hip during the first three months post pelvic fracture will help with the early stages of rehabilitation. Electrical stimulation is a treatment machine that uses an electrical current to cause a single muscle or a group of muscles to contract. This contraction helps strengthen injured muscles and helps with the healing process. It can also help with pain relief by blocking pain signals from the brain. After a pelvic fracture they are surgically fixed and will be advised not to put any weight on the operated leg for 10 weeks. During this time hip muscles become very weak as they will not be used as much as normal. Bed exercises can help keep muscle strength but this study would like to try using electrical stimulation machines alongside bed exercises to see if it can improve muscle strength even more. Electrical stimulation machines are already used by rehabilitation. Electrical stimulation is a treatment machine that uses an electrical current to cause a single muscle or a group of muscles to contract. This contraction helps strengthen injured muscles and helps with the healing process. It can also help with pain relief by blocking pain signals from the brain. After a pelvic fracture they are surgically fixed and will be advised not to put any weight on the operated leg for 10 weeks. During this time hip muscles become very weak as they will not be used as much as normal. Bed exercises can help keep muscle strength but this study would like to try using electrical stimulation machines alongside bed exercises to see if it can improve muscle strength even more. Electrical stimulation machines are already used by patients to increase muscle strength. Participants will be put into one of two groups, both groups will be given an electrical stimulation machine but one will be on a placebo setting. Participants will need to use the machine twice a day along with their bed exercises and will need to fill in a diary when and how many times the machine has been used for 10 weeks until their 12 week appointment with the orthopaedic consultant. The participants weight bearing status will change and they will be asked to perform a muscle strength test on both the operated and nonoperated leg. They will also have their walking quality assessed. The results will compare both groups for muscle strength and walking changes.

NCT ID: NCT03289858 Completed - Hip Fractures Clinical Trials

Randomized Controlled Trial for Exparel Hip Fracture

Start date: September 1, 2017
Phase: Phase 4
Study type: Interventional

This is a prospective, randomized study looking at the effect that a long-acting local anesthetic has on pain control in patients having surgery for hip fractures. The investigators are conducting the study to see if that reduces the amount of pain medicine needed after surgery, and if it reduces other medical complications after surgery.

NCT ID: NCT03278834 Completed - Trauma Clinical Trials

NMES and Pelvic Fracture Rehabilitation

Start date: January 1, 2014
Phase: N/A
Study type: Interventional

Objectives: The acute care of pelvic fractures has improved recently however there are no formal guidelines for rehabilitation of these types of fractures. Patients have long periods of non-weight bearing causing muscle wastage. Neuromuscular electrical stimulation (NMES) has proven to minimise muscle loss. However, this has not previously been investigated within this patient population. Design: Double blind, randomised, feasibility study. Setting: NHS trust hospital setting. Participants: Nine patients with surgically fixed pelvic fractures were randomly allocated at six weeks post fracture. Interventions: The intervention group completed six weeks of NMES. The placebo group used transcutaneous electrical nerve stimulation (TENS). Main outcome measures: Peak torque (Nm) was calculated in the operated limb at 12 weeks using the non-operated limb as a baseline. Compliance and intensity levels were recorded. Feasibility of NMES was evaluated using a feasibility questionnaire. Pain was measured at six and 12 weeks using a visual analogue scale (VAS).

NCT ID: NCT03275129 Completed - Hip Fractures Clinical Trials

Ultrasound Assessment of Heart and Lungs for Hip Fracture Procedure

Start date: May 28, 2018
Phase: N/A
Study type: Interventional

The investigators would like to investigate whether performing ultrasound assessments in patients undergoing surgery for hip fractures is able to identify previously undiagnosed heart or lung conditions. The investigators would like to determine whether information provided by this ultrasound assessment is significant enough to alter the anesthetic management plan of these patients. This study has the potential to demonstrate that ultrasound could be used as a diagnostic bedside tool in the perioperative period, possibly altering standard of care for this patient population.

NCT ID: NCT03268356 Completed - Hip Fractures Clinical Trials

STRONG - Study of AGN1 LOEP for the Treatment of the Contralateral Femur After Fragility Fracture

Start date: August 15, 2017
Phase: N/A
Study type: Interventional

To evaluate the procedure and safety profile of the AGN1 Femoral LOEP Kit. This pilot study will be used to evaluate AGN1 Femoral LOEP treatment in a contralateral proximal femur during hip fracture repair.

NCT ID: NCT03266874 Active, not recruiting - Clinical trials for Rheumatoid Arthritis

G7 BiSpherical Acetabular Shell PMCF Study

Start date: December 10, 2017
Phase:
Study type: Observational

The primary objective of this study is to obtain implant survivorship and clinical outcomes data for the commercially available G7 BiSpherical Acetabular Shell.

NCT ID: NCT03265275 Completed - Hip Fractures Clinical Trials

Why Still in Hospital After Hip Fracture Surgery?

Start date: September 11, 2017
Phase:
Study type: Observational

At our institution, hip fracture patients are admitted and treated according to a fast track patient pathway. The aim of this study is to identify areas of this patient pathway that can be improved. To achieve this, the study will investigate the underlying reasons for the continued need for hospitalization on the consecutive days after hip fracture surgery.

NCT ID: NCT03251469 Recruiting - Hip Fractures Clinical Trials

Single Dose of Tranexamic Acid and Blood Loss, in Elderly Patients With Hip Fracture

Start date: January 2013
Phase: Phase 2
Study type: Interventional

The aim of this study is to investigate the hypothesis that single dose of tranexamic acid (TXA) preoperatively will lower blood loss and transfusion rate in elderly patients with hip fractures (intertrochanteric or Subcapital), that will be treated with intramedullary nailing and cemented hemiarthroplasty respectively. After application of inclusion and exclusion criteria, patients will be randomized in two groups. Group 1 will include patients that receive preoperatively single dose of TXA (15mg/kg) and Group 2 will include patients that receive normal saline (control group).

NCT ID: NCT03247205 Withdrawn - Clinical trials for Cognitive Impairment

Hip Fracture Exercise and Rehabilitation Post Hip Fracture Study

HipERS
Start date: August 2018
Phase: N/A
Study type: Interventional

This pilot study will look at whether it is possible to give better physical therapy to people with cognitive limitations who have had a hip fracture.