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Fractures, Bone clinical trials

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NCT ID: NCT03196258 Terminated - Pain, Postoperative Clinical Trials

Cognitive Behavioural Therapy to Reduce Persistent Post-Surgical Pain After Fracture

SPOC_CBT
Start date: October 1, 2018
Phase: N/A
Study type: Interventional

Psychological factors such as stress, distress, anxiety, depression, and poor coping strategies may be associated with ongoing pain following injuries such as fractures. In order to study this relationship, researchers at McMaster University have developed the Somatic Pre-Occupation and Coping (SPOC) questionnaire, which identifies illness beliefs that may help to predict which patients are at risk for ongoing pain, reduced quality of life, and delays in returning to work and leisure activities after a fracture requiring surgical treatment. Previous research using the SPOC questionnaire suggests the possibility that fracture patients with illness beliefs that put them at risk for developing ongoing pain could be identified early in the treatment process. These patients may benefit from cognitive behavioural therapy (CBT) which is designed to modify such thoughts with the goal of reducing ongoing pain and improving quality of life. The goal of this study is to determine if CBT is effective in reducing ongoing pain and improving quality of life in fracture patients who show illness beliefs that may place them at risk for developing ongoing pain.

NCT ID: NCT03195179 Completed - Surgery Clinical Trials

Primary Urethral Realignment Versus Suprapubic Cystostomy After Pelvic Fracture Urethral Injury

Start date: January 1, 2016
Phase:
Study type: Observational

Pelvic fracture urethral injuries (PFUI) occur in up to 10% of pelvic fractures. It remains controversial whether initial urethral realignment after PFUI decreases rates of urethral obstruction and the need for subsequent urethral procedures. The retrospective record review should determine the utility of acute urethral realignment after PFUI.

NCT ID: NCT03193697 Completed - Clinical trials for Intertrochanteric Fractures

Efficacy and Safety of Cemented and Cementless Prostheses for Unstable Intertrochanteric Fractures in the Elderly

Start date: January 1, 2014
Phase: N/A
Study type: Interventional

This trial explores the application of different hip replacement materials in elderly patients with unstable intertrochanteric fracture, and aims to provide the experience and basis for hip arthroplasty in elderly osteoporosis patients with unstable intertrochanteric fracture.

NCT ID: NCT03192683 Completed - Pediatric ALL Clinical Trials

Modified "Providence" Pedi Cast-Sling vs.Cast and Sling

Start date: April 1, 2016
Phase: N/A
Study type: Interventional

Examining custom made sling vs. off the shelf sling for immobilization following pediatric upper extremity fractures.

NCT ID: NCT03186963 Completed - Clinical trials for Radius Fracture Distal

Effectiveness of Immobilization in the Postoperative Analgesia of Surgically Treated Distal Radius Fractures

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

The purpose of this study is to determine wether postoperative immobilization is effective in controlling the pain of patients with intra-articular distal radius fractures treated with volar locking plate fixation. The study hypotheses is that postoperative immobilization does not enhance the analgesia of these patients.

NCT ID: NCT03185663 Completed - Femoral Fractures Clinical Trials

Pilot Study Comparing Two Techniques of Taking Care Analgesic in Patients 70 and Older, Awaiting Surgery After Extracapsular Fracture of the Proximal Femur

ALGOFRACT
Start date: August 31, 2017
Phase: N/A
Study type: Interventional

The fracture of the proximal femur is a common traumatic pathology in patients aged over 70 years, associated with a mortality of 20 to 30% a year. The care is delayed emergency. During this wait, the occurrence of heel pressure ulcers is regularly found, despite wearing antiescarres slippers. Mobilization, source of pain, is also problematic. 759/5000

NCT ID: NCT03184896 Active, not recruiting - Hip Fractures Clinical Trials

Services Mapping Among Older Adults With Hip Fracture

HiFit
Start date: November 14, 2018
Phase:
Study type: Observational

Hip fracture is a osteoporosis-related fracture with higher mortality, and is a major public health issue in China. The British Orthopedic Association and the British Geriatric Society have published the UK Blue Book, which summarizes current evidence and best practice in the hip fracture care and secondary prevention, but this kind of standardized practice in hip fracture care is not yet existed in China. The Blue Book standards will be used as the most contemporary evidence-based guidelines for management of hip fracture.This study is to prospectively examine the barriers and facilitators in the current management of hospital in China by comparing the Blue Book standards.

NCT ID: NCT03182751 Completed - Hip Fractures Clinical Trials

Does Early Administration of Tranexamic Acid Reduce Blood Loss and Perioperative Transfusion Requirement

Start date: April 2, 2018
Phase: Phase 2
Study type: Interventional

Intertrochanteric hip fractures typically result in blood loss from the fracture and require surgery that can cause further blood loss. This study is being done to look at a medication called tranexamic acid which may reduce blood loss and the need for blood transfusions associated with surgery.

NCT ID: NCT03182608 Completed - Hip Fractures Clinical Trials

Ultrasound Assessment of the Anatomic Landmarks for Spinal Anesthesia in Patients With Hip Fracture

Start date: June 9, 2017
Phase: N/A
Study type: Interventional

Investigators assess the anatomic landmarks for spinal anesthesia in patients with hip fracture using ultrasonography.

NCT ID: NCT03178799 Enrolling by invitation - Clinical trials for Osteoporosis Fracture

Randomized Fracture Liaison Services

Start date: June 23, 2017
Phase:
Study type: Observational

Aims: To compare clinical outcomes for patients under FLS and usual care at the NTUH MH and BB. Method: Four hundred subjects with new hip fracture or newly identified vertebral fracture are randomly assigned into FLS and usual care (UC). FLS subjects received osteoporosis-related assessments, treatments, consultations on diet, medications, exercise, fall preventions given mainly by care managers with followed up telephone call at 4, 8, 12, 18, 24 months then annually for up to 10 years. Care managers will perform baseline assessments and follow them by telephone annually for up to 10 years for UC subjects. Major outcomes include bone mineral density assessment rate, calcium, vitamin D, and osteoporosis medication initiation and adherence rate, fall and fracture incidences, mortality, and healthcare resource utilizations.