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Orthopedic Disorder clinical trials

View clinical trials related to Orthopedic Disorder.

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NCT ID: NCT04244942 Recruiting - Orthopedic Disorder Clinical Trials

CERAMENTâ„¢| Bone Void Filler Device Registry

Start date: March 30, 2020
Phase:
Study type: Observational [Patient Registry]

A device registry to compile data on the performance of CERAMENT BONE VOID FILLER in normal use.

NCT ID: NCT04243135 Completed - Orthopedic Disorder Clinical Trials

r-ESWT in Moderate Knee Osteoarthritis

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

This study aims to compare the efficacy of r-ESWT treatment with sham-ESWT on pain, walking speed, physical function, and isokinetic muscle strength in knee osteoarthritis.

NCT ID: NCT04225949 Withdrawn - Orthopedic Disorder Clinical Trials

Patients Understanding of PROM Graphs

Start date: May 15, 2021
Phase: N/A
Study type: Interventional

This study evaluates patients' ability to understand PROM scores when presented in graphs. One half will receive one version of the survey, while the other half will receive a second version of the survey.

NCT ID: NCT04222166 Completed - Orthopedic Disorder Clinical Trials

Registry of Amniotic Membrane: Evaluating Utilization and Outcomes in Various Applications

Start date: December 16, 2019
Phase:
Study type: Observational [Patient Registry]

This registry will assess clinical outcomes following the use of Cryopreserved Amniotic Membrane (CAM) for the treatment of orthopedic and various other conditions. This registry will collect outcomes data via a registry of up to 100 patients who have received treatment with CAM in the post-market setting. Patients will be enrolled from up to five healthcare centers.

NCT ID: NCT04196166 Completed - Orthopedic Disorder Clinical Trials

Routine Preoperative Evaluation in Surgical Patient

Start date: January 1, 2014
Phase:
Study type: Observational

The "routine" pre-operative tests in healthy orthopaedic patients undergoing intermediate/ major surgery are not justified. In this study of 670 healthy orthopedic patients with 7610 preoperative tests, investigators found that surgical plan was influenced in <1% of patients. Surgeons should be sensitized to reconsider this practice particularly with limited resources.

NCT ID: NCT04190719 Recruiting - Clinical trials for Cardiovascular Diseases

Patient Empowerment for Major Surgery Preparation @ Home

Paprika
Start date: January 3, 2020
Phase: N/A
Study type: Interventional

Non-randomized monocentric open cohort study vs historical comparative group testing the efficacy of a multimodal prehabilitation program (based on physical activity, nutritional support and mental preparation) for unfit patients based on nutrition, physical activity and mental preparation in reducing postoperative complications in elective major surgery

NCT ID: NCT04173377 Recruiting - Orthopedic Disorder Clinical Trials

Elbow Outcomes Clinical Study (WELBOW)

WELBOW
Start date: June 8, 2020
Phase:
Study type: Observational

WELBOW study is an international, ambispective and prospective, single arm, multicenter, observational, non-comparative, Post-Market Clinical Follow-up (PMCF).

NCT ID: NCT04138264 Completed - Orthopedic Disorder Clinical Trials

Opioid Counseling Following Orthopaedic Surgery

Start date: June 19, 2018
Phase: N/A
Study type: Interventional

Postoperative pain management and opioid consumption following outpatient orthopaedic surgery may be influenced by a number of variables including knowledge of safe opioid use. A prospective randomized study is designed to understand the effect of preoperative opioid counseling on postoperative opioid consumption and the typical opioid consumption patterns following common outpatient orthopaedic surgeries. The hypothesis was that patients who received preoperative opioid counseling will consume less postoperative opioid medication and experience greater satisfaction with pain management.

NCT ID: NCT04090372 Completed - Orthopedic Disorder Clinical Trials

Digital Preop-planning of Total Hip Arthroplasties

PLANORTHO
Start date: January 8, 2020
Phase: N/A
Study type: Interventional

Residual leg length discrepancy is a common issue after total hip arthroplasty(THA). Digital preoperative planning may improve the accuracy of the surgical procedure and may help the surgeon to precisely predict implants sizes

NCT ID: NCT04078880 Completed - Anemia Clinical Trials

Iron Supplementation in Hip/Knee Surgery

Start date: December 4, 2018
Phase: N/A
Study type: Interventional

Randomized controlled trial to evaluate the efficacy of oral iron supplementation in reducing the prevalence of preoperative anemia in a cohort of 82 patients undergoing elective prosthetic hip or knee surgery.