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Hip Fracture clinical trials

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NCT ID: NCT06389279 Not yet recruiting - Hip Fracture Clinical Trials

The Effect of Facial Plane Blocks on Postoperative Recovery Quality in Hip Surgery

Start date: April 24, 2024
Phase:
Study type: Observational

The aim of this study was to evaluate the effect of ultrasound-guided pericapsular nerve block, fascia iliaca compartment block, and femoral block on the quality of recovery as part of multimodal analgesia before hip surgery under spinal anesthesia.

NCT ID: NCT06146205 Not yet recruiting - Hip Fracture Clinical Trials

The Hip Fracture Surgical Approach Trial

HIFSAT
Start date: January 2024
Phase: N/A
Study type: Interventional

The HIFSAT study will compare the standard direct lateral approach to hemiarthroplasty to a new muscle sparing approach (SPAIRE) in femoral neck fracture patients.

NCT ID: NCT05425355 Not yet recruiting - Surgery Clinical Trials

Intravenous vs Oral Acetaminophen in Postoperative Hip Fracture Adult Patients

INTACT-HIP
Start date: November 4, 2022
Phase: Phase 4
Study type: Interventional

The INTACT-HIP trial study will evaluate feasibility of conducting a randomized, double-blinded controlled trial comparing postoperative treatment with intravenous (IV) acetaminophen versus oral acetaminophen, in older adults undergoing hip fracture surgery. The results of this feasibility trial will be used to inform designing a larger, multi-center, randomized controlled trial to assess the efficacy of IV acetaminophen compared to oral acetaminophen to reduce delirium and improve other clinical and patient-centered outcomes after hip fracture surgery. It will randomize 42 older adults to receive either oral or IV acetaminophen after hip fracture surgery.

NCT ID: NCT04165538 Not yet recruiting - Hip Fracture Clinical Trials

Thromboelastography (TEG) and Clopidogrel Withdrawal Time in Elderly Patients With Hip Fracture

Start date: January 2020
Phase: N/A
Study type: Interventional

In the elderly patients with hip fracture, some often take antiplatelet drugs such as clopidogrel due to the ischemic cardiovascular or cerebrovascular diseases. In traditional practice, these patients often need to stop medication for 5-7 days before surgery. But on the other hand, delayed surgery will lead to a significant increase in fracture related complications. Therefore, the appropriate time for drug withdrawal is particularly important in this population. Thromboelastography is a monitoring method that can accurately judge the anticoagulation status of patients. We hope to use thromboelastography to guide the time of drug withdrawal, shorten the time of drug withdrawal as much as possible, and reduce the incidence of fracture related complications without increasing the risk of massive hemorrhage.

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

NCT ID: NCT02428868 Not yet recruiting - Anemia Clinical Trials

IV Iron in Association With Tranexamic Acid for Hip Fracture

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

It is a prospective randomized controlled study aiming to test if tranexamic acid combined to intravenous iron before and after surgery for hip fracture in elderly can decrease peri-operative red cell transfusion.

NCT ID: NCT02428257 Not yet recruiting - Hypotension Clinical Trials

Continuous Spinal Anesthesia With Hypobaric Bupivacaine to Preserve Hemodynamics in Elderly

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

The study evaluates the potential beneficial effects on hemodynamics when hypobaric bupivacaine is used instead of isobaric bupivacaine in continuous spinal anesthesia for surgical repair of hip fracture in elderly patients. Half of the patients will receive hypobaric bupivacaine and the over half will reveive isobaric bupivacaine and hemodynamic data will be compared.

NCT ID: NCT02133794 Not yet recruiting - Hip Fracture Clinical Trials

Tomosynthesis Use in Detecting Subtle Occult Hip Fractures

Start date: June 2014
Phase: N/A
Study type: Interventional

The purpose of this project is to determine if using tomosynthesis, in conjunction with x-ray, is better at detecting hip fractures than using x-ray alone. The goal of this study will be to include the use of tomosynthesis with x-ray as usual practice when a patient comes to the emergency room with symptoms of a hip fracture.

NCT ID: NCT01084122 Not yet recruiting - Hip Fracture Clinical Trials

Efficacy and Safety of Intravenous Iron Sucrose in Patients With Hip Fracture to Prevent Perioperative Anemia

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

The purpose of this study is to evaluate the safety and efficacy of intravenous iron sucrose in patients with hip fracture and surgical intervention to prevent perioperative anemia.

NCT ID: NCT00860132 Not yet recruiting - Hip Fracture Clinical Trials

Economic Aspects Associated With the Implementation of an Orthogeriatric Setting in a General Hospital

Start date: May 2009
Phase: N/A
Study type: Observational

The economic and social burden of hip fractures is expected to increase dramatically, but financial resources remain limited. This calls for the investigation of innovative new forms of organization and integration of medical, surgical and rehabilitation services for these patients. The study will investigate economical aspects associated with implementation of a comprehensive orthogeriatric ward for elderly hip fracture patients in a general hospital, compared with the classic model of orthopedic treatment followed by rehabilitation period.