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Spinal Surgery clinical trials

View clinical trials related to Spinal Surgery.

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NCT ID: NCT03512379 Recruiting - Safety Clinical Trials

Clinical Trial for the Application of Robotic System in Spinal Surgery

Start date: August 1, 2015
Phase: N/A
Study type: Interventional

This randomized controlled study was designed to evaluate the accuracy, safety and clinical outcomes of the robot assisted spinal surgery.

NCT ID: NCT03501810 Recruiting - Spinal Surgery Clinical Trials

Study Assessing Safety and Performance of OrtoWell Distractor in Patients Undergoing Spinal Surgery

Start date: April 5, 2018
Phase:
Study type: Observational

Study to Assess the Safety and Performance of the OrtoWell® Distractor in Patients Undergoing Spinal Surgery

NCT ID: NCT03160170 Terminated - Surgical Blood Loss Clinical Trials

Efficacy of Suction Enabled Retraction Device

Start date: June 20, 2017
Phase: N/A
Study type: Interventional

This is a prospective randomized controlled trial of the Suction-Integrated Surgical Tissue Elevator & Retractor [SISTER] device to assess: - Effects on operative time and efficiency of exposure in open lumbar spine cases. - Effect on total blood loss during the exposure part of the operation. - Rate of clogging of suction device.

NCT ID: NCT03069794 Completed - Spinal Surgery Clinical Trials

Effect of Spinal Surgery on the Posture and the Balance of the Patients Reached of Spinal Pathologies

Start date: March 28, 2017
Phase: N/A
Study type: Interventional

Many studies are in favour of the importance of the rachis on the postural balance of the body.It is possible to study the upright posture by determining the center of pressure using a platform of strength.The spinal surgery have two objectives ,mechanic and neurologic .By deformation correction and stabilizing vertebral stages via arthrodesis, it seems to hypothesize that surgery can modify postural balance. This study aim to evaluate spinal surgery effect on posture using that plaftorm .

NCT ID: NCT02892617 Completed - Spinal Surgery Clinical Trials

Evaluation of the Prevalence of Germs Slow Growth in the Intervertebral Disc (IVD) During Spinal Surgery

DISCO-PROP
Start date: December 2014
Phase: N/A
Study type: Observational

Low back pain is one of the most frequent reasons for consultation in rheumatology. There is a strong correlation between low back pain, and the presence of a type of Modic 1 signal on MRI. The anomaly Modic 1 results in a hypointense signal T1-weighted images and hyperintense on T2-weighted sequences (including T2 STIR and / or Fat Sat) and contrast enhancement of the endplates after gadolinium injection; it corresponds to a replacement of normal cancellous bone of fibrovascular tissue. The origin of this inflammatory process Modic 1 into the vertebra is still unknown. infectious hypothesis was raised, including contamination by germs called "slow-growth" such as Propionibacterium acnes (PA). Many studies interesting Bacteriological analysis of disc material found the presence of bacteria (prevalence between 0 and 54%). A recent clinical trial evaluating the efficacy of antibiotic treatment compared to placebo in low back pain with Modic 1; a show effectiveness of this treatment on the different clinical parameters evaluated. However skin contamination is not formally excluded, particularly in patients previously infiltrated (including epidural). Our hypothesis is that the slow-growing bacteria are not involved in Modic 1 type of disc disease, and the possible presence of PA or other slow-growing bacteria in samples obtained discal posterior approach would be related to intraoperative contamination or during preoperative spinal infiltrations The main objective is to assess the prevalence of germs slow growth in the intervertebral disc in the spinal surgery by anterior disc disease in type 1 Modic.

NCT ID: NCT02678156 Completed - Craniotomy Clinical Trials

Assessment of the Performance of LYoplant® ONlay for Duraplasty

LYON
Start date: April 2016
Phase:
Study type: Observational

The aim of this Post Market Clinical Follow-up Study is to collect clinical data on the performance of Lyoplant® Onlay. To assess the performance of the product, various safety and efficacy parameters have been selected.

NCT ID: NCT02595788 Recruiting - Obesity Clinical Trials

Haemodynamic Changes During Anaesthesia in the Prone Position, Evaluated Using Transoesophageal Ultrasound

Start date: March 2014
Phase: N/A
Study type: Observational

Transoesophageal ultrasound examination before and after prone position.

NCT ID: NCT01988818 Completed - Knee-surgery Clinical Trials

Prospective, Randomized Study of 2 Different Wound Dressings

Close
Start date: April 2014
Phase: N/A
Study type: Interventional

The primary objective of this investigation is to evaluate the performance of a self-adhesive absorbent post-operative dressing coated with a soft silicone layer in minimize the risk of the development of blistering in subjects after hip or knee arthroplasty or spinal surgery in comparison to a standard wound dressing The secondary objectives are to evaluate: - the performance of the dressing - the comfort, conformability and the acceptability of the dressing - pain before, during and after dressing removal - the overall cost regarding dressing wear time, time to do dressing change and personal resources needed

NCT ID: NCT01855542 Completed - Spinal Surgery Clinical Trials

The Aim of This Investigation is to Compare the Influence of 0.9% Saline and Plasmalyte Solution on Acid-base Balance and Electrolytes in Healthy Patients Undergoing Major Spine Surgeries.

Start date: March 2012
Phase: N/A
Study type: Interventional

Chloride-rich isotonic crystalloid solutions have been shown to exert electrolyte imbalance and metabolic acidosis in critically ill patients. The aim of this investigation is to compare the influence of 0.9% saline and plasmalyte solution on acid-base balance and electrolytes in healthy patients undergoing major spine surgeries.

NCT ID: NCT01356082 Completed - Cardiac Surgery Clinical Trials

CNAP™ Monitor Study

Start date: May 2011
Phase: N/A
Study type: Observational

A newly developed monitor for continuous non-invasive blood pressure monitoring (CNAP™ Monitor 500; CNSystems Medizintechnik AG, Graz, Austria) provides beat-to-beat BP readings and is non-invasive. To make sure that anaesthesiologist can rely on and make clinical decisions based on values provided by the CNAP™ monitor, to demonstrate its reliability we will test it during the perioperative care of children.