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Post-laminectomy Syndrome clinical trials

View clinical trials related to Post-laminectomy Syndrome.

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NCT ID: NCT02641223 Completed - Clinical trials for Post-laminectomy Syndrome

Evaluation of Objective Outcomes With the Use of an Activity Tracker During the Trial Period of Spinal Cord Stimulation

Start date: November 2015
Phase: N/A
Study type: Observational

For this study the investigators will conduct five-day trial periods for spinal cord stimulator (SCS) effectiveness—once a patient is deemed to be a possible SCS candidate, the trial leads are implanted and they are asked to return to clinic in five days to evaluate the effectiveness of the trial. The primary outcome for this study will be a comparison of daily energy expenditure (EE), in units of kcal/day, prior to and after the trial implantation of the SCS leads and external pulse generator. Patients will wear the accelerometer device twenty-four hours a day for five days prior to the trial lead implantation to obtain baseline values, have the trial leads implanted in the procedure clinic, then continue to wear the accelerometer for another five days. Baseline and post-SCS energy expenditure values will be compared. The secondary outcomes for this study will be steps taken, hours of sleep, and Oswestry Disability Index (ODI, as described in appendix 1) during the pre and post trial implantation periods. SCS itself is not a research procedure in this study, rather it is part of routine medical care for patients who would benefit from the procedure.

NCT ID: NCT01990287 Terminated - Low Back Pain Clinical Trials

SENSE (Subcutaneous and Epidural Neuromodulation System Evaluation) Study

Start date: November 2013
Phase: N/A
Study type: Interventional

The purpose of the study is to demonstrate safety and efficacy of spinal cord stimulation with peripheral nerve field stimulation for the treatment of chronic low back and leg pain.

NCT ID: NCT01818297 Terminated - Clinical trials for Failed Back Surgery Syndrome

Subcutaneous Nerve Stimulation for Failed Back Surgery Syndrome (FBSS) Patients

Start date: April 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to assess the safety and efficacy of Subcutaneous Nerve Stimulation (SQS) (also known as Peripheral Nerve Stimulation [PNS]) in the reduction of chronic, intractable post-surgical back pain in adults.