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Active clinical trials for "Hip Fractures"

Results 431-440 of 655

Internal Fixation or Joint Replacement Therapy for Aged Hip Fracture Patients

Intertrochanteric Fractures

To evaluate the efficacy and safety of internal fixation or arthroplasty for hip fracture patients over 75 years of age with multiple medical complications through the operation time, intraoperative bleeding, time to start weight bearing activities and other indicators.

Unknown status10 enrollment criteria

Pertrochanteric Fracture Fixation In Elderly Adults Using Proximal Femoral Nail Anti-rotation (HERACLES)...

Pertrochanteric FractureIntertrochanteric Fractures4 more

This is a prospective case series of elderly adult patients sustaining pertrochanteric fractures who will be treated by a proximal femoral nail with a non-helical (straight) blade. This study seeks to observe and evaluate the outcomes, advantages and complication rates in using the HERACLES PFN with a non-helical (T-shaped parallel) blade.

Unknown status12 enrollment criteria

Does Limb Pre-Conditioning Reduce Pain After Hip Arthroscopy

Hip InjuriesHip Dislocation1 more

The purpose of this study is to determine if the utilization of Ischemic Pre-Conditioning 24-hours prior to hip arthroscopy decreases patient's post-operative pain and opioid consumption.

Unknown status2 enrollment criteria

Post Market Clinical Follow-Up of the Zimmer Stafit Acetabular System

OsteoarthritisHip7 more

This study is a Post Market Clinical Follow up study to fulfil the post market surveillance obligations according to Medical Device Directive and European Medical Device Vigilance System (MEDDEV) 2.12-2. The data collected from this study will serve the purpose of confirming safety and performance of the Zimmer Stafit Acetabular System.

Terminated8 enrollment criteria

Treatment of Sub-capital Fractures of Hip Joint by Using TriboFit™ Acetabular Buffer

Hip Fractures

The purpose of this study is to determine the performance and efficacy during 6 and 12 month post operation. determine changes in patient pain level determine changes in patient functionality determine changes in patient life quality

Terminated16 enrollment criteria

Patients With Acute Hip Fractures Will Receive Either the PENG Block or no Block Respectively.

Hip Fractures

Hip fracture pain is often severe and traditionally managed by systemic opioids which have increased risk of side effects in frail elderly patients. Inadequately controlled pain may lead to delirium which increases mortality and morbidity. The overall aim of this RCT is to investigate the potential for improved pain relief accomplished by the addition of the PENG block to current standard practice of pre-operative analgesia (systemic morphine), compared to the control group, which involves no block (operator will still go through the motion as if performing a block) plus standard pre-operative analgesia. The investigator hypothesize that the addition of a single shot PENG block at the side of hip fracture in addition to traditional systemic morphine provides good preoperative pain relief on movement and reduces the need for breakthrough opioid requirements. The investigator hypothesize that the interventional group dynamic pain score assessed at 30 minutes after the block compared to control group dynamic pain score at 30 minutes after the "block" will be at least a 3 point difference between the 2 groups .

Unknown status16 enrollment criteria

PENG: an Estimation of ED50 in Neck of Femur Fracture

Hip FracturesPain1 more

The effective dose of local anaesthetic used in PENG blocks to achieve analgesia in patients with fractured neck of femur is unknown. It is planned to address this question using a dixon/massey sequential dosing methodology to establish the ED50 of 0.25% Bupivacaine.

Unknown status10 enrollment criteria

Evaluation of the Performance of Y-STRUT® Medical Device to Strengthen Pre-fractural Tumour-induced...

Pathological Fracture of HipBone Metastases

HIPPON 100 is a national, multicentre, prospective, retrospective, descriptive and non-interventional study, in patients having a Y-STRUT® medical device implanted to prevent a high risk of impending pathological fracture. The primary objective of this study is to evaluate the performance of the studied medical device by measuring the frequency of patient with a fracture at the implantation site within 1 year after implantation. A total of 100 patients from France will be enrolled (until November 2018) and followed up to 24 months.

Terminated6 enrollment criteria

Ultrasound Guided Femoral Nerve Block

Hip Fracture

The goal of the study is to evaluate whether pain control achieved by Ultrasound Guided Femoral Nerve Blockade (USFNB) is equal in efficacy to standard pain management practice of parenteral injection of opioid pain medication in patients presenting to the emergency department (ED) with hip fracture.

Unknown status7 enrollment criteria

In Vivo Hip Fracture Discrimination With Quantitative Computed Tomography (QCT)

OsteoporosisProximal Femur Fracture

Numerous geometric and bone mineral density (BMD) parameters can be derived from quantitative computed tomography (QCT) images of the proximal femur analyzed using dedicated software. The primary objective is to evaluate the contribution of QCT-image analysis to the prediction of the osteoporotic hip fracture risk, as compared to the reference standard, namely, dual energy X-ray absorptiometry (DXA). Study hypothesis: For predicting osteoporotic hip fracture, findings from QCT images of the proximal femur analyzed using dedicated software are superior over DXA measurements of proximal femoral BMD.

Terminated21 enrollment criteria
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