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Spinal Diseases clinical trials

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NCT ID: NCT05425680 Recruiting - Clinical trials for Degenerative Lumbar Spine Diseases

Remote Intelligent Interactive Virtual Reality Assessment in Patients With Degenerative Lumbar Spine Diseases

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

This study will combine virtual reality (VR) technology with machine learning to focus on functional movement. Patients' symptoms will be evaluated, and exercise instruction with real-time feedback will be provided. The goals of this research are to: (1) develop a waist digital sensor for real-time monitoring as an evaluation tool, (2) apply a real-time monitoring system in conjunction with virtual reality for telerehabilitation, and (3) develop the standard model.

NCT ID: NCT05405374 Recruiting - Clinical trials for Degenerative Disc Disease

OSTEOAMP Lumbar Fusion Intra-Patient Controlled Study

SELECT
Start date: May 6, 2022
Phase: N/A
Study type: Interventional

The objective of this clinical study is to compare OSTEOAMP SELECT Fibers to Infuse Bone Graft, in terms of effectiveness and safety, when used as a bone graft substitute in in skeletally mature patients qualified for 2-lumbar interbody fusion (LIF) by means of an intra-patient control model.

NCT ID: NCT05332249 Recruiting - Surgery Clinical Trials

Registry for Degenerative Spinal Disease (RDSD)

RDSD
Start date: March 8, 2021
Phase:
Study type: Observational [Patient Registry]

The outcome after spinal surgery is important and the evidence is critical to develop treatment. The purpose of this study is to make a prospective registry of database for further research.

NCT ID: NCT05287867 Recruiting - Clinical trials for Degenerative Disc Disease

Trial for Treating Painful Degenerative Disc Disease

Start date: May 6, 2022
Phase: N/A
Study type: Interventional

To evaluate and compare two platelet-based treatments of the functional spinal unit spaced 4 weeks apart to sham procedures for the treatment of degenerative disc disease.

NCT ID: NCT05214235 Recruiting - Diabetes Mellitus Clinical Trials

A Clinical Study on the Effect of Hypoglycemic Drugs on the Prognosis of Spinal Surgery in Diabetic Patients

Start date: February 7, 2022
Phase:
Study type: Observational

Diabetes mellitus is a group of metabolic diseases caused by multiple etiologies and characterized by chronic hyperglycemia. It seriously harms human health and has become a global public health challenge. Diabetes mellitus is present in 5% to 25% of patients undergoing spine surgery, and the prevalence has been increasing over the past decade. It is worth noting that spinal surgery for patients with diabetes has significant risks, mainly manifested in the significant increase of postoperative complications such as wound infection, delayed healing and wound hematoma, which seriously affect the long-term prognosis of patients' quality of life, spinal function and stability of internal fixation. Research shows that hypoglycemic drugs can not only control blood glucose level, but also affect the stability of nerve, bone and internal fixation, which is expected to improve the prognosis of spinal surgery in patients with diabetes. Metformin and sitagliptin are widely used hypoglycemic drugs. Studies have shown that metformin can increase bone mineral density in patients and have a protective effect on bones. Sitagliptin induces macrophage polarization of the M2 phenotype and reduces the impaired behavior of osteoblasts on titanium (TI) implants in a dose-dependent manner, thereby enhancing the bone regeneration required for successful orthopedic and dental implants in diabetic patients. However, the effects of these two drugs on the long-term prognosis of diabetic patients after spinal surgery, such as quality of life, spinal function and stability of internal fixation, have not been reported. This investigation is a prospectie cohort study. The purpose of this study is to determine whether metformin and sitagliptin are associated with patient-reported outcomes and internal fixation stability at one year following elective spine surgery. Providers may use this information to help patients who need elective spinal surgery choose hypoglycemic drugs and to counsel patients with diabetes on expectations following spine surgery.

NCT ID: NCT05146583 Recruiting - Lumbar Disc Disease Clinical Trials

Injection of Autologous Bone Marrow Aspirate in Patients With Degenerative Disc Disease.

Start date: November 1, 2021
Phase:
Study type: Observational

Lumbar discectomy and injection of purified cellular bone marrow concentrate or lumbar discectomy only

NCT ID: NCT05101057 Recruiting - Clinical trials for Degeneration of Cervical Intervertebral Disc

A Retrospective Study to Examine the Effect of CMF Stimulation on Primary ACDF Patients

Start date: November 15, 2021
Phase:
Study type: Observational

A retrospective parallel group comparison study to support expansion of the indication of the company's FDA approved Spinalogicâ„¢ device to include the cervical spine. The SpinalogicTM device was initially approved by FDA as an adjunct to one- or two-level lumbar fusion (P910066/S011). It is a non-invasive bone growth stimulator (BGS) that generates a combined magnetic field (CMF) that has been proven to accelerate bone healing and fusion in the lumbar spine.

NCT ID: NCT05082090 Recruiting - Clinical trials for Spinal Disorders/Injuries

A Multi-Center Post-Market Data Collection Protocol to Evaluate the Performance of Orthofix Spine Devices

RWE Spine
Start date: September 15, 2021
Phase:
Study type: Observational

This protocol is designed to study Orthofix regulatory approved and commercially available spine devices to generate Real World Evidence (RWE) of device safety and performance in the treatment of patients with spine injuries and/or disorders following the local medical standard of care. The clinical data generated from this study will support compliance to global regulatory requirements including but not limited to the European Medical Device Regulation (EU MDR) for the applicable devices.

NCT ID: NCT04825522 Recruiting - Spine Disease Clinical Trials

The Effect of Intrawound Vancomycin Powder in Spine Surgery

Start date: March 27, 2022
Phase: Phase 4
Study type: Interventional

Problem: Postoperative wound infection following various spinal surgeries is a serious complication. The incidence of post-surgical wounds in spine surgery is high, and various researchers have reported different infection rates. In addition, increased healthcare costs, prolonged lengths of stay in hospital, and reduced quality of life as a result of surgical site infections (SSI) are also major concerns. Several methods for avoiding SSI, such as betadine irrigation, vacuum-assisted closure, and intra-wound vancomycin powder, have been used to reduce the rate of wound infection in spine surgery. Use of local vancomycin has been popular because of its protective effects and lower cost. According to some reports, prophylactic administration of intra-wound vancomycin powder before wound closure is an effective method for decreasing postoperative wound infection rates; however, other studies have revealed a non-significant effect of intra-wound vancomycin use for decreasing the postsurgical wound infection rate. Solution: Therefore, the investigators will prospectively randomize all various types of spinal surgeries to patients who will receive intrawound vancomycin powder and control group who will not receive the powder and to see it's effect in reducing the post-surgical infection.

NCT ID: NCT04820816 Recruiting - Clinical trials for Orthopedic Disorder of Spine

Effect of Posterior Pelvic Tilt on Balance and Sensory Integration in Patients With Non-specific Low Back Pain

Start date: September 1, 2020
Phase:
Study type: Observational [Patient Registry]

There is a debate in the literature about the effect of NSLBP on pelvic tilt and its effect on balance, sensory integration and functional disability so we need this study to fill the aforementioned gap in literature in this field. So the purpose of the study is to evaluate posterior pelvic tilt effect on overall dynamic balance, sensory integration and functional disability in patients with non-specific low back pain.