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Hip Fractures clinical trials

View clinical trials related to Hip Fractures.

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NCT ID: NCT05677061 Completed - Clinical trials for Intertrochanteric Fractures

Clinical Evaluation on HA Coated Dynamic Hip Screws for Trochanteric Femoral Fractures

Start date: April 2008
Phase: N/A
Study type: Interventional

Evaluated whether HA coated dynamic hip screws can improve fixation of the screw in trochanteric femoral fractures

NCT ID: NCT05673486 Completed - Hip Fractures Clinical Trials

Regional Anesthesia by PENG-Block in Emergency Department

ED-PENGBLOCK
Start date: March 31, 2023
Phase: N/A
Study type: Interventional

The study is a single-centre, open-label randomized comparative trial. Adult patients admitted to the emergency department for a hip fracture will be enrolled. Pericapsular nerve block (PENG-block) is a regional anesthesia technique developed primarily as an analgesic technique in a perioperative setting during hip fractures related surgical procedures. Some authors propose the use of PENG-Block as an alternative to fascia iliaca block and femoral block for the analgesic management of hip fracture in the emergency department, but scientific evidence is weak in this setting. The hypothesis of this study is that the use of PENG Block in the emergency department provides a better pain management for patients suffering from hip fractures with less opioid use.

NCT ID: NCT05660603 Recruiting - Hip Fractures Clinical Trials

Circum-Psoas Blocks Versus Combined Lumbar and Sacral Plexus Blocks in Hip Fracture Surgery

Start date: December 20, 2022
Phase: N/A
Study type: Interventional

Hip fracture (HF) is one of the major worldwide problems that constitute a significant mortality rate, ranging from 14- 36% in the first year after injury, and is associated with profound temporary and sometimes permanent impairment of independence and quality of life in the geriatric population. Surgical treatment is considered the best option for patients with hip fractures,s especially in the elderly, however, it is associated with moderate to severe postoperative pain. Pain is one of the main factors limiting ambulation, increasing the risk of thromboembolism by immobility and causing metabolic changes that affect other systems. Therefore, individualized pain management with the use of appropriate analgesic techniques is of paramount importance. Moreover, early intervention of rehabilitation aiming at a better postoperative recovery may reduce the length of hospital stay and return to daily. Effective pain management is one of the crucial components in enhanced recovery after surgery (ERAS). • Numerous regional anesthetic techniques have been used to provide analgesia following hip fracture surgery, including intrathecal morphine, epidural analgesia, fascia iliaca block, lumber plexus block, and sacral plexus block, however, each of these techniques has specific limitations that prevent them from being the analgesic technique of choice for hip fracture surgery. To our knowledge, there is no study done to compare circum-psoas block versus the combined lumbar and sacral plexus blocks as pre-emptive analgesia in patients undergoing hip fracture surgery under general anesthesia.

NCT ID: NCT05606042 Recruiting - Acetabular Fracture Clinical Trials

Curvafix® Intramedullary System for Fixation of Pelvic and Acetabular Fractures, A Post Market Evaluation

Start date: November 24, 2021
Phase:
Study type: Observational

Prospective, single arm, post-market evaluation to evaluate the use and performance of the IM Implant in a post market setting.

NCT ID: NCT05602155 Completed - Clinical trials for Femur Intertrochanteric Fractures

Partial Weight Bearing Proximal Femoral Nail Due to Intertrochanteric Fracture.

randomized
Start date: August 1, 2018
Phase:
Study type: Observational

Femur intertrochanteric fractures (FITC) are one of the most common fractures of the lower extremity, caused by osteoporosis, caused by minor trauma in elderly patients. Today, it is successfully treated with proximal femoral nails (PFN) designed in different ways. After surgical fixation with PFN, patients are mobilized by placing full weight, but some complications can be seen due to the patients being osteoporotic. In this study, the investigators planned to investigate the effect of full weight bearing and partial weight bearing on complications, which were not previously described in the literature.

NCT ID: NCT05587244 Enrolling by invitation - Clinical trials for Rheumatoid Arthritis

G7 Freedom Constrained Vivacit-E Liners

Start date: May 8, 2023
Phase: N/A
Study type: Interventional

The main objectives of this study are to confirm the long-term safety, performance, and clinical benefits of the G7 Freedom Constrained Vivacit-E Acetabular Liners in primary and revision total hip arthroplasty.

NCT ID: NCT05581901 Completed - Pain, Postoperative Clinical Trials

Perioperative Methadone in Hip Fracture Patients

Start date: January 12, 2023
Phase: Phase 4
Study type: Interventional

Postoperative analgesic treatment needs to be improved. Numerous studies suggest that a single dose of Methadone given during surgery significantly ameliorates postoperative pain and reduces postoperative opioid consumption. Perioperative methadone is already used in isolated cases such as patients with chronic pain or patients with high morphine tolerance. However, it is not routinely used in the elderly and fragile, and there is insufficient reliable evidence on this treatment and population. Further investigation is highly relevant and necessary.

NCT ID: NCT05567523 Completed - Hip Fractures Clinical Trials

Safety Study of Dexmedetomidine in Elderly Under General Anesthesia

Start date: June 1, 2019
Phase: Phase 4
Study type: Interventional

The purpose of this study is to find out appropriate dose range of dexmedetomidine to provide the elderly patients satisfactory sedation and analgesia with stable hemodynamics during perioperative period of hip replacement under general anesthesia.

NCT ID: NCT05564741 Not yet recruiting - Anesthesia Clinical Trials

Acute Hip Fracture and Spinal Anaesthesia Injection Time

Start date: October 2022
Phase: Phase 4
Study type: Interventional

The systemic effects of spinal anesthesia is not fully known. Our aim of this study is to assess whether there is a difference in hemodynamic effects if the spinal dose is given fast (15s) or slow (90s) in elderly patients with acute hip fracture (AHF). Ninety (n=90) patients with AHF planned for surgery within 72h at our hospital will be enrolled in the study and randomly devided into two groups. The patients will receive one predetermined dose of spinal anesthesia followed by an advanced minimally-invasive hemodynamic monitoring through an arterial line using FloTrac-system. The hemodynamic parameters will be conducted 10 minutes prior to the spinal anaesthesia and 30 minutes after the spinal block is given. Hypotension was defined as a fall in MAP > 30 % or a MAP <65mmHg.

NCT ID: NCT05559736 Recruiting - Clinical trials for Femoral Neck Fractures

Artemis Proximal Femoral Nail for Internal Fixation of Intertrochanteric Femur Fractures

Start date: May 24, 2023
Phase: N/A
Study type: Interventional

In February 2021, Altior Trauma Innovations™ announced that it had received 501(k) FDA approval for the Artemis Proximal Femoral Nail (PFN) System for internal fixation of intertrochanteric femur fractures. The objective of this pilot study is to evaluate safety, efficacy and feasibility of the Artemis PFN implant for operative fixation of intertrochanteric femoral fractures, compared to matched historical control patients who received other implants.