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Hip Fractures clinical trials

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NCT ID: NCT02788994 Recruiting - Clinical trials for Unilateral Unstable Hip

Stabilization of Fresh Unilateral Unstable Pertrochanteric Hip Fracture

PET
Start date: June 2016
Phase: N/A
Study type: Interventional

This is a preliminary study to establish the issues and potential of the investigators proposed project, which involves recruitment of patients with and without dementia, who have been admitted to hospital following hip fractures. The study will be evaluating the result of treatment of unstable pertrochanteric hip fractures focusing on how soon mobility is restored leading to their independence. These patients would require surgical fixation (not replacement) of their hip fractures. The study will evaluate two methods of fixation of hip fractures treated with either a pin (nail) which is inserted within the cavity of the thigh bone or a hip screw with a plate which is applied on the outer aspect of the thigh bone. The data collected from this study will provide information on whether one method of fixation is better than the other.

NCT ID: NCT02787031 Completed - Anesthesia Clinical Trials

Variations in Anesthesia Care for Hip Fracture Surgery

Start date: April 2002
Phase: N/A
Study type: Observational

The investigators will use health administrative data to examine the variation of anesthesia type for hip fracture surgery, as well as sources of variation and predictors of variation.

NCT ID: NCT02780076 Active, not recruiting - Clinical trials for Femoral Neck Fractures

Recovery of Physical Functioning After Hip Fracture

HIPFRAC
Start date: May 30, 2016
Phase: N/A
Study type: Interventional

The survivors after hip fracture often report severe pain and loss of physical functioning. The poor outcomes cause negative impact on the person's physical functioning and quality of life and put a financial burden on society. It is important to continue and progress the functional training that already started at the hospital, while the patients are transferred to short-term stays in a nursing home before they are returning to home. The aim presently is to examine the effects of a functional training program by a RCT design, initiated by the physiotherapist and performed by the nurses, on physical functioning while the patients are at short term stays in primary health care.

NCT ID: NCT02774148 Terminated - Hip Fracture Clinical Trials

Pain Control in Elderly Hip Fracture Patients: Is Intravenous Acetaminophen Superior to Oral Administration?

Start date: December 2016
Phase: Phase 4
Study type: Interventional

The primary objective is to determine if intravenous acetaminophen decreases pain scores and the amount of morphine equivalence received as compared to oral acetaminophen in patients greater than 65 years old after sustaining a hip fracture.

NCT ID: NCT02753010 Completed - Gastroparesis Clinical Trials

Gastric Emptying in Elderly With Hip Fracture

GASEMPHIP
Start date: March 2011
Phase: Phase 2
Study type: Observational

The gastric emptying of 400 ml 12.6% carbohydrate rich drink is investigated in elderly women, age 75-100, with acute hip fracture. The emptying time will be assessed by the paracetamol absorption technique, and lag phase and gastric half-emptying time compared with two gender-matched reference groups: elective hip replacement patients, age 45-71, and healthy volunteers, age 28-55.

NCT ID: NCT02738073 Recruiting - Hip Fracture Clinical Trials

Effects of Tranexamic Acid on Blood Loss and Transfusion Requirement Following Hip Fracture

Start date: n/a
Phase: N/A
Study type: Interventional

Tranexamic acid (TA) inhibits fibrinolysis by binding to lysine binding-sites of plasminogen to fibrin. Fibrinolysis is stimulated by surgical trauma, and the administration of TA has been shown effective in decreasing blood loss both intra-operatively and in the immediate post-operative period in elective hip and knee arthroplasty patients. Both the timing and dosing of TA has been investigated in these patients. Subsequent blood transfusion rate has also been shown to decrease as result of TA administration. Despite the support for TA utilization that exists in the arthroplasty literature, the data is scarce regarding its administration during surgical treatment of hip fractures. This is patient population who is at high risk for transfusion due to symptomatic post-operative anemia. This study aims to investigate whether TA's advantageous effects in the arthroplasty patient population can be extrapolated to the more unstable, heterogeneous hip fracture patient population. If the study is able to show a difference in blood loss and transfusion requirement, the long term implications of this with regards to cost and mortality can be significant.

NCT ID: NCT02736383 Completed - Hip Fracture Clinical Trials

Tranexamic Acid in Hip Fracture Surgery

Start date: May 2016
Phase:
Study type: Observational

To determine if TXA utilization is effective at reducing transfusion rates in elderly patients undergoing surgery for treatment of a hip fractures.

NCT ID: NCT02718976 Completed - Pain, Postoperative Clinical Trials

Shamrock - Ultrasound/MR Image Fusion Guided Lumbar Plexus Block

Start date: March 2016
Phase: Phase 2
Study type: Interventional

The main objective is to complete a double-blinded randomized controlled crossover trial of lumbar plexus block with the Shamrock technique guided by ultrasound (US)/magnetic resonance imaging (MRI) image fusion vs. the Shamrock technique guided by ultrasound in healthy volunteers. The investigators will assess block procedure-related parameters, anatomical spread of local anesthetic, and motor and sensory effects.

NCT ID: NCT02699619 Completed - Hip Fractures Clinical Trials

Undisplaced Femoral Neck Fractures 2 Hansson Pins or 3 Pins Interlocked in Plate (Pinloc) Using RSA

Start date: March 2016
Phase: N/A
Study type: Interventional

Femoral neck fractures represent about half of the hip fractures and are further divided into displaced and undisplaced fractures. Displaced femoral neck fractures are almost always treated surgically with arthroplasty. However there is an ongoing debate on which implant is superior for undisplaced fractures. A novel implant design (Pinloc) has been developed by Swemac Innovation AB. While the original implant consisted of 2 isolated hook pins, the modified design consists of 3 titanium hook pins interlocked in an aluminum plate. Interlocking is a new principle of implant design and improves fixation and load transfer amongst the pins. The superiority of the modified design is so far only proven preclinically. The role of the Pinloc in clinical use remains unclear. Investigators are planning a randomized controlled trial on undisplaced femoral neck fractures to establish a method for implanting the tantalum markers, to observe the fracture healing process and to further investigate the role of the Pinloc.

NCT ID: NCT02699502 Not yet recruiting - Hip Fracture Clinical Trials

Metabolic Therapy in Patients With Osteoporosis After Hip Fracture by an Orthopedic-rehabilitation-metabolic Team

Start date: March 2016
Phase: N/A
Study type: Interventional

Metabolic therapy in patients with osteoporosis after hip fracture by cooperation orthopedic-rehabilitation-metabolic: Determination of drug treatment regardless of reaching the follow-up clinic