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Active clinical trials for "Intervertebral Disc Displacement"

Results 81-90 of 352

Post-marketing Clinical Follow-up of the Medical Device DIVA®

Lumbar Disc Herniation

Observational, ambispective, longitudinal, comparative, open, multicentric study. The main objective is to compare the performance of care in patients operated with and without DIVA®.

Recruiting8 enrollment criteria

Pain Monitoring of Herniated Disc Surgery Patients With Oura Ring

Pain Measurement

The objective of this research study is to show whether data given by Oura ring could be used to objectively measure patients pain and well-being before and after disc surgery.

Recruiting2 enrollment criteria

The Spine PROMCO Study

Lumbar Disc HerniationSpondylolisthesis1 more

Our primary objective is to design a cohort to determine the treatment outcome of different surgical interventions of the degenerative lumbar spine highlighting the expediency and value of the current surgical treatment program.

Recruiting10 enrollment criteria

PMCFU of an Annular Closure System

Lumbar Disc Herniation

The purpose of this retrospective chart review study is to collect the data that will be used to provide clinical evidence to support the post-market surveillance program.

Recruiting2 enrollment criteria

Impact of Muscle Degeneration in Chronic Low Back Pain

Lumbar Spinal StenosisLumbar Disc Herniation2 more

Surgical interventions for the removal of intervertebral disc fragments or to enlarge a narrow spine canal are commonly performed worldwide and are considered efficient. Concomitant low back pain is not uncommon among patients with lumbar nerve compression and neurological symptoms. When present, controversy persists in the literature regarding its ideal management. Although neurological symptoms improve after decompressive surgery, the presence of residual chronic low back pain may worsen satisfaction scores and cause functional disability. The hypothesis of the present study is that the presence of atrophy of the paraspinal and trunk muscles predicts chronic low back pain after lumbar neural decompression. If confirmed, this finding will aid in better planning of physical rehabilitation strategies for this group of patients, as well as a clearer prediction regarding surgical treatment outcomes for patients and health professionals.

Recruiting9 enrollment criteria

Application of 3D Printing Guide Plate in Percutaneous Disc Decompression

Lumbar Disc HerniationRadiculopathy5 more

Application of 3D printing guide plate in percutaneous disc decompression

Not yet recruiting15 enrollment criteria

Su Jok Application in After Lumbar Disc Surgery

PainPostoperative3 more

Surgical treatment is applied in 15% of individuals diagnosed with lumbar disc herniation. In this study, it was aimed to determine the effect of Su Jok application, which is one of the non-drug methods, in reducing or completely eliminating pain and anxiety after lumbar disc surgery and increasing the quality of recovery.The universe of the study, between November 2022 and June 2023, Istanbul Kartal Dr. Patients with lumbar disc surgery will be recruited in the Neurosurgery Clinic of Lütfi Kırdar City Hospital. Data will be obtained with Introductory Information Form, McGill Pain Scale Short Form (SF-MPQ), Visual Analog Scale (Visual Comparison Scale) (VAS), STAII State Anxiety Scale, Quality of Recovery Questionnaire (QOR-40). The individual who will undergo lumbar disc surgery will be visited in the clinic one day before the surgery and will be informed about the study. The sampled individuals will be included in the intervention and control groups using a random number table created with MS Excel software. Su Jok will be applied to the patients included in the intervention group at the third hour after the operation. Before the application, Quality of Recovery Questionnaire (QOR-40), McGill Pain Scale Short Form and STAII State Anxiety Scale will be administered. After the application, the pain levels of the patients will be re-evaluated with the Visual Analogue Scale (Visual Comparison Scale) (VAS) and their anxiety levels will be re-evaluated with the STAII State Anxiety Scale. On the first and second days after the surgery, the patients will be visited again in the clinic and the Quality of Healing Questionnaire (QOR-40), Visual Analog Scale (Visual Comparison Scale) (VAS) and STAII State Anxiety Scales will be administered before the Su Jok application, and then the Su Jok application will be repeated.After the application, the pain levels of the patients will be re-evaluated with the Visual Analogue Scale (Visual Comparison Scale) (VAS) and their anxiety levels will be re-evaluated with the STAII State Anxiety Scale. Patients will be interviewed again at the control appointment 10 days after discharge, and their quality of recovery will be determined using the Quality of Healing Questionnaire (QOR-40). In the control group, pain, anxiety and healing quality levels will be determined in the same periods without any application.

Not yet recruiting13 enrollment criteria

Application of 3D Printing Guide Plate in Endoscopic Spinal Surgery

Lumbar Disc HerniationLumbar Spinal Stenosis2 more

Application of 3D printing guide plate in endoscopic spinal surgery

Not yet recruiting15 enrollment criteria

Comparison of the Effect of Lumbar Traction, Spinal Manipulation, and Surgery in the Treatment of...

Lumbar Disc HerniationLumbar Traction2 more

To compare the effect of lumbar traction, lumbar spinal manipulation and lumbar surgery in the treatment of LDH.

Terminated6 enrollment criteria

Ozone Therapy in Patients on Waiting List for Surgery Due to Disc Herniation: Prospective, Post-authorization...

Lumbar Herniated Disc

The main objective of this study is to estimate the cost-effectiveness of ozone therapy in patients on the waiting list for surgery due to disc herniation.

Active14 enrollment criteria
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