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Hip Fractures clinical trials

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NCT ID: NCT02016859 Not yet recruiting - Clinical trials for Critically Ill Patients

Observational Prospective Study of the Predicted Value of Immature Thrombocytes Counts in Three Different Groups of Critically Ill Patients

Start date: January 2014
Phase: N/A
Study type: Observational [Patient Registry]

Immature Platelet Fraction (IPF) is a new value in CBC blood tests Recent Studies showed that this value may be another prognostic factor in critically ill patients such as those admitted to ICU, or those with neutropenic Fever. The purpose of the study is to check if the IPF may be used as a prognostic Factor in these patients

NCT ID: NCT01984385 Completed - Hip Fractures Clinical Trials

Hip Fracture Impact on Vascular Events In Noncardiac Surgery patIents: a cOhort evaluatioN (Hip VISION): Pilot Study

Start date: December 2013
Phase: N/A
Study type: Observational [Patient Registry]

Hip VISION (Pilot Study) is a Prospective Observational Cohort Study to evaluate the incidence of overall and cause-specific mortality among consecutive patients aged ≥ 18 years presenting with hip fracture to the Juravinski Hospital of the Hamilton Health Sciences. This pilot study will assess the feasibility of a larger prospective international cohort study. After eligibility has been confirmed and informed consent has been obtained, participants will be registered in the study. Troponin level, complete blood counts and serum creatinine level will be collected at day 1 through day 10 post admission. CAM instrument will be employed at admission and once daily post admission day 1 through day 10. FIM Instrument will be administered within 72 hours of admission to establish pre-fracture functional independence and disability. Patients will be contacted by research personnel by telephone 30 days after study registration.

NCT ID: NCT01961895 Completed - Hip Fractures Clinical Trials

Lumbar Plexus Block Upon the Incidence of Ischemic Cardiovascular Events in Elderly Patients With Hip Fracture

Start date: May 2010
Phase: Phase 4
Study type: Interventional

The purpose of this study is evaluate the efficacy of perioperative continuous lumbar plexus block in reducing the risk of cardiac ischemic events of elderly patients undergoing surgery for hip fractures, expressed as a reduction of ischemic events per subject.

NCT ID: NCT01950169 Completed - Hip Fracture Clinical Trials

Effects of Bisphosphonates and Nutritional Supplementation After a Hip Fracture

Start date: December 2004
Phase: N/A
Study type: Interventional

The study hypothesis is that nutritional supplementation together with bisphosphonates have a better preserving effect on bone mineral density (BMD) after hip fracture than bisphosphonates alone and that nutritional supplementation given postoperatively for 6 months preserve lean body mass in elderly hip fracture patients.

NCT ID: NCT01940536 Withdrawn - Hip Fracture Clinical Trials

The Effect of Tranexamic Acid on Transfusion Rates in Intertrochanteric Hip Fractures

Start date: December 2015
Phase: Phase 4
Study type: Interventional

The goal of this study is to determine if the use of tranexamic acid, a safe and effective antifibrinolytic, in patients with intertrochanteric hip fractures will result in a reduction in blood transfusion rates. Treatment will be administered pre-operatively as well as at the time of surgical incision. The primary outcome will be need for blood transfusion. Secondary outcomes will include calculated perioperative blood loss, length of stay, cost of inpatient care, and rate of adverse events, including DVT, PE, infection, MI, cerebrovascular event, need for re-hospitalization or re-operation and 30 day mortality.

NCT ID: NCT01934946 Recruiting - Hip Fracture Clinical Trials

Rehabilitation Care for Hip Fracture

Start date: September 2013
Phase: N/A
Study type: Interventional

Purpose: Hip fracture is a common disease on elderly. They become disabled easily if no adequate rehabilitation was given. The aim of the study is to compare the effectiveness of different types of post acute rehabilitation care for hip fracture.

NCT ID: NCT01930409 Completed - Hip Fracture Clinical Trials

Back to the Future: Bridging the Hospital to Home Continuum After Hip Fracture

B2F
Start date: November 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether is is feasible and acceptable to deliver a telephone based coaching intervention compared with education alone in community dwelling older adults (age 60 and older) after a fall related hip fracture.

NCT ID: NCT01908751 Terminated - Clinical trials for Femoral Neck Fractures

Fixation Using Alternative Implants for the Treatment of Hip Fractures (FAITH-2)

FAITH-2
Start date: September 2014
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine the impact of surgical fixation (cancellous screws versus sliding hip screws) and biologic intervention (Vitamin D versus placebo) on patient important outcomes.

NCT ID: NCT01904071 Completed - Hip Fracture Clinical Trials

Ultrasound Guided Pain Control Versus Standard Treatment in Emergency Department HIP Fracture Patients

Start date: October 2008
Phase: Phase 4
Study type: Interventional

Hip Fracture (HFx) is a painful injury that is often treated in the Emergency Department (ED) with intravenous opiates. However, this class of medications may cause deleterious side effects. An alternative analgesic approach involves regional anesthesia. The investigators attempted to determine (1) whether ultrasound guided peripheral nerve blocks (UPNBs) could be safely performed in an ED setting, (2) whether UPNBs would be more effective than standard treatment in controlling pain from HFx and (3) which of two UPNBs was superior for pain relief. A convenience sample of patients with an isolated HFx and a pain score > 5/10 were enrolled and randomized to one of three arms: (1) Ultrasound guided 3-in-1 femoral nerve block (UFNB), (2) Ultrasound guided fascia iliaca compartment block (UFIB), or (3) IVMS. Patients indicated their pain from 0 (no pain) to 10 (extreme pain).

NCT ID: NCT01850251 Terminated - Hip Fractures Clinical Trials

Effects of a Supplement Enriched in Hydroxymethylbutyrate and Vitamin D on Muscle Strength in Hip Fracture

Start date: June 2013
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether a nutritional supplement high in protein and energy, and enriched with hydroxymethylbutyrate (HMB) and vitamin D is more effective than a standard nutritional supplement high in protein and energy in improving muscle strength in elderly patients with hip fracture.