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Orthopedic Disorder clinical trials

View clinical trials related to Orthopedic Disorder.

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NCT ID: NCT05212324 Not yet recruiting - Orthopedic Disorder Clinical Trials

Management of Congenial Clasped Thumb

Start date: February 11, 2022
Phase:
Study type: Observational

Congenital clasped thumb is a rare progressive flexion and adduction deformity presenting with heterogenous congenital abnormalities.(1, 2) It is confused with trigger finger deformity due to fixated flexion deformity of the thumb. In congenital trigger finger entrapment is present at A1 pulley level due to fusiform enlargement of flexor pollicis longus tendon

NCT ID: NCT05194774 Not yet recruiting - Orthopedic Disorder Clinical Trials

Greater Trochanter Epiphysiodesis In Hip Pathology

Start date: January 2022
Phase:
Study type: Observational

One of the most common problems in the treatment of pediatric patients with various disorders of the hip joint is the formation of deformity of the proximal femur, such as abnormal growth of the greater trochanter, which causes it to be positioned high in relation to the femoral head. This condition is called "relative overgrowth of the greater trochanter" (ROGT).

NCT ID: NCT04811313 Not yet recruiting - Orthopedic Disorder Clinical Trials

Tranexamic Acid in Pediatric Undergoing Proximal Femoral Osteotomies and/or Acetabular Osteotomy

Start date: May 2021
Phase: N/A
Study type: Interventional

Surgical hip reconstruction reduces the hip joint through soft tissue releases and osteotomies of the femur and/or pelvis. Blood loss and subsequent blood transfusion are normal consequences of hip reconstruction.

NCT ID: NCT04768088 Not yet recruiting - Clinical trials for Anterior Cruciate Ligament Injuries

Training of Falling Techniques on Landing Mechanics

Start date: January 1, 2022
Phase: N/A
Study type: Interventional

The overall purpose of this study is to quantify the effect and retention of one-week training of falling techniques on landing biomechanics associated with anterior cruciate ligament (ACL) loading compared to soft-landing techniques in young recreational athletes. The secondary purpose is to assess the safety of the training program. Aim 1: To quantify the effect of one-week training of falling techniques on landing biomechanics during forward, lateral, vertical, and diagonal landings compared to soft-landing techniques. We hypothesize that falling techniques will result in increased knee flexion angles and decreased landing forces, knee abduction and internal rotation angles, and knee moments for all landing directions compared to soft-landing techniques immediately after the training. Aim 2: To assess the retention effects of the falling techniques on landing biomechanics compared to soft landings. We hypothesize that the effects of falling techniques on ACL loading variables will be more highly retained compared to soft-landing techniques two weeks after the training. Aim 3: To identify the safety of the training program. We hypothesize that participants can complete the training without suffering minor, moderate, or major injuries, while occasional minor bruises might be observed.

NCT ID: NCT04668430 Not yet recruiting - Orthopedic Disorder Clinical Trials

Evaluation of Personalized Biomechanical Models of the Musculoskeletal System Before and After Orthopedic Surgeries

OrthosimPro
Start date: December 15, 2020
Phase: N/A
Study type: Interventional

Advances in biomechanical modeling of musculoskeletal systems make it possible to consider the use of a digital clone of a patient to test surgical procedure before carrying it out on the patient himself. The study aims at evaluating the design and simulation procedure of anatomical and functional pre and post surgical patient-specific numerical models.

NCT ID: NCT04601376 Not yet recruiting - Orthopedic Disorder Clinical Trials

Testing of Mobile Monitoring System

Start date: June 2024
Phase: N/A
Study type: Interventional

We will complete a prospective, observational study comparing the accuracy of the mobile monitoring tool on identifying SSI compared to manual review.

NCT ID: NCT04546594 Not yet recruiting - Pain Clinical Trials

Epidemiological Data on Pain

ALGOBASES
Start date: October 2020
Phase:
Study type: Observational

The ALGOBASES project is an observational epidemiological study of pain through the collection of pain evaluation questionnaires and information with the aim of creating a descriptive "pain" evaluation in all patients who need to benefit from orthopedic, thoracic or gynecological surgery. The painful symptomatology will thus be evaluated in all its dimensions (demographic data, physical, psychological, socio-cultural components) and linked to the pathology justifying the specialized care. It is planned to collect the same data at each subsequent event in order to allow the determination of predictive factors, pain trajectories according to the type of surgery, and the profile of subjects at risk of acute or chronic postoperative pain.

NCT ID: NCT03899298 Not yet recruiting - Stroke Clinical Trials

Safety and Clinical Outcomes With Amniotic and Umbilical Cord Tissue Therapy for Numerous Medical Conditions

Start date: September 1, 2019
Phase: Phase 1
Study type: Interventional

To determine the safety and efficacy of Amniotic and Umbilical Cord Tissue for the treatment of the following condition categories: Orthopedic, Neurologic, Urologic, Autoimmune, Renal, Cardiac and Pulmonary Conditions. The hypotheses are that the treatments are not only extremely safe, but also statistically beneficial for all conditions. Outcomes will be determined by numerous valid outcome instruments that compile general quality of life information along with condition-specific information as well.

NCT ID: NCT03453905 Not yet recruiting - Bone Metastases Clinical Trials

Evaluation of the Ability of CT-based Finite Element Analysis (CTFEA) to Predict Fractures in Patients With Metastases: a Randomized Controlled Study.

ZYCTFEA
Start date: March 1, 2018
Phase: N/A
Study type: Interventional

Patients with metastases to proximal femur, who are evaluated fr the risk of pathologic fracture in order to decide on preventive fixation vs follow-up constitute the study population. The patients will be randomized in two arms. First arm - the decision of treatment will rely on conventional decision algorithm including specialist judgement and Mirels' score. Second arm- the decision on treatment will be supported by CTFEA analysis of bone structure and quantitative simulation-based estimate of fracture risk, in addition to the conventional decision algorithm. Operation rates, pathologic fracture rates and additional secondary outcomes will be compared between the two study arms.