Clinical Trials Logo

Fractures, Bone clinical trials

View clinical trials related to Fractures, Bone.

Filter by:

NCT ID: NCT03031015 Completed - Clinical trials for Closed Fracture of Finger

Cemented K-wire Fixation vs Plating for Finger Fractures

CKFPFF
Start date: January 1, 2011
Phase: N/A
Study type: Interventional

To introduce a novel external-fixation technique using the combination of K-wires and cement. For comparison, we also included another group of patients who were treated using a mini plate and screw system. Bone healing, range of motion of the fingers, costs of treatments, and patient satisfaction were assessed.

NCT ID: NCT03026920 Recruiting - Clinical trials for Fracture Dislocation

Pelvic and Acetabular Fracture in Old People

Start date: June 2016
Phase: N/A
Study type: Interventional

It was reported that satisfactory postoperative outcome was difficult to obtain for the pelvic or acetabular fracture in old people. The less invasive surgical method was conducted in this study. Then, the clinical results were compared with the patients treated using traditional methods to assess the less invasive method.

NCT ID: NCT03026868 Recruiting - Clinical trials for Fracture Dislocation

Novel Quadrilateral Surface Plate for Acetabular Fracture

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

The novel plate could be used to manage acetabular fractures involving quadrilateral surface and posterior column, which may lower the intraoperative blood loss and reduce complication rate.

NCT ID: NCT03024008 Recruiting - Bone Fracture Clinical Trials

Enhancement of Bone Regeneration and Healing in the Extremities by the Use of Autologous BonoFill-II

Start date: July 27, 2017
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this clinical study is to evaluate the safety and the efficacy of BonoFill-II as an autologous bone-regenerating graft in the reconstruction of deficient bone in two clinical indications: 1. Long and short bone extra-articular comminuted fracture 2. Long and short bones extra and intra articular defect /Gap or non-union, incapable of self-regeneration

NCT ID: NCT03023956 Completed - Clinical trials for Humeral Fracture, Proximal

Outcome of Proximal Humerus Fractures :Anatomic Neck Fractures vs Surgical Neck Fractures

Start date: July 2016
Phase: N/A
Study type: Observational

From April ,2014 to April 2015,31 patients with fractures of the proximal humerus were treated in our hospital. According to anatomic neck fractures (ANF) and surgical neck fractures (SNF), we divided the patients into two groups. All the patients were followed at least 1 year.

NCT ID: NCT03020563 Withdrawn - Clavicle Fracture Clinical Trials

Does Liposomal Bupivacaine Provide Improved Pain Management for ORIF of Midshaft Clavicle Fractures?

Start date: August 23, 2017
Phase: Phase 4
Study type: Interventional

To determine whether liposomal bupivacaine wound infiltration decreases pain scores and narcotic use when compared to bupivacaine alone after open reduction internal fixation of midshaft clavicle fractures.

NCT ID: NCT03017105 Terminated - Clinical trials for Proximal Humerus Fractures (to be Managed Non-operatively)

Cross-education for Proximal Humerus Fracture Rehabilitation

Start date: January 2017
Phase: Phase 1/Phase 2
Study type: Interventional

Proximal humerus fractures (break of the top part of the upper arm bone) are common in older people with poorer bone quality. Often patients do not undergo surgery for these fractures: the bone fragments may be in an acceptable enough position to be able to heal naturally, or the patient may not be well enough medically to undergo an operation. These patients need to wear a sling to immobilise their injured shoulder, however muscles start to weaken quickly when they are unable to be used. This research project will look at whether strength-training the opposite/uninjured limb, known as "cross education", has any effect on preserving the function of the injured/fractured limb. Participants will be randomised into two groups using minimisation, that is to say the groups will have balanced numbers in terms of exact pattern of fracture and gender. One group will receive traditional rehabilitation exercises and treatment by the physiotherapist for their injured limb; the other group will receive the same but in addition will also undergo a strength-training exercise programme for their uninjured limb. Only qualified physiotherapists with experience of treating this patient cohort will be involved. Sessions in the physiotherapy department will last up to 30 minutes each and will comprise of: patient review, exercise progression, and advice giving/question answering; home exercise programmes will be expected to be completed 2-3 times daily and last up to 30 minutes each; number of sessions will be agreed between the participant and treating physiotherapist with treating ending once an agreed, acceptable level of function has been achieved. The Oxford Shoulder Score patient-reported outcome measure will be completed by the participant at 6 and 12 weeks and the European Quality of Life (EuroQoL)-5D-5L at 12 weeks after commencement of treatment.

NCT ID: NCT03014024 Completed - Colles' Fracture Clinical Trials

Low-level Laser Therapy in Distal Radius Fractures

Start date: December 2016
Phase: N/A
Study type: Interventional

Conservative treatment of distal radius fracture is immobilisation with cast for 4-6 weeks. After removing the cast, it is common to still have pain, swelling and reduced mobility in the wrist. The aim of this study is to evaluate the influence of LLLT on the hand.

NCT ID: NCT03011047 Not yet recruiting - Clinical trials for Orbital Floor Fracture

Efficacy of Endoscopic Transantral Surgical Approach in the Repair of Orbital Blow-Out Fractures

Start date: August 18, 2017
Phase: N/A
Study type: Interventional

Aim of this study is to assess the efficacy of endoscopic trans-maxillary surgical approach versus traditional trans-orbital surgical approach (control group) in orbital blow out fractures in terms of postoperative clinical and digital radio-graphical assessments.

NCT ID: NCT03009890 Completed - Clinical trials for Radius Distal Fracture

Surgery vs. Casting for Displaced Articular Radius Fractures in Elderly

DART
Start date: February 1, 2017
Phase: N/A
Study type: Interventional

Objective: to compare the functional outcome after open reduction and internal fixation with non-operative cast treatment for elderly patients with displaced intra-articular distal radius fractures.