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Cervical Stenosis clinical trials

View clinical trials related to Cervical Stenosis.

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NCT ID: NCT05717010 Completed - Clinical trials for Cervical Disc Disease

Is There a Risk of Perioperative Stroke Due to the Retraction Used During Anterior Cervical Discectomy?

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

In anterior cervical disc surgery, head and neck extansion position and, surgical retraction used while reaching the anterior surface of the cervical vertebra can be affect the carotid blood flow and constituting a risk for cerebral ischaemia. In this study, we planned to investigate the relationship between head position and retraction, cerebral oxygenation and postoperative cognitive functions in patients undergoing anterior cervical disc surgery.

NCT ID: NCT05404412 Completed - Clinical trials for Lumbar Spinal Stenosis

The Impact of Contrast Media Used in Epidural Steroid Injections on Thyroid Function Tests

Start date: June 1, 2022
Phase:
Study type: Observational [Patient Registry]

This study is aim to disclose the effect of contrast media, which used in epidural steroid injections, on the parameters of thyroid function tests (TFTs). The patients who underwent an epidural steroid injection were included. The investigators hypothesized that contrast media owing to contain iodine may impair the values of TFTs.

NCT ID: NCT05356286 Recruiting - Spondylosis Clinical Trials

Recording of Intraoperative Spinal Cord Stimulation and Monitoring

Start date: January 21, 2011
Phase: N/A
Study type: Interventional

Opioid overdose suppresses brainstem respiratory circuits, causes apnea, and may result in death. Epidural electrical stimulation (EES) at the cervical spinal cord facilitated motor activity in rodents and humans, and we hypothesized that EES of the cervical spinal cord could antagonize opioid-induced respiratory depression in humans. In this study, we will stimulate the spinal cord during surgery and assess its effects on respiratory function in human patients.

NCT ID: NCT05066711 Enrolling by invitation - Clinical trials for Cervical Radiculopathy

NuVasive® ACP System Study

Start date: May 22, 2022
Phase:
Study type: Observational

The primary objective of this study is to evaluate the safety and performance of anterior cervical spine surgery using the NuVasive anterior cervical plate (ACP) System as measured by reported complications, radiographic outcomes, and patient-reported outcomes (PROs).

NCT ID: NCT04684901 Enrolling by invitation - Spondylolisthesis Clinical Trials

Effectiveness of AlloWrap® for the Reduction of Inflammation in ACDF Procedures

Start date: January 18, 2021
Phase: N/A
Study type: Interventional

The primary objective of this study is to obtain evidence of the effectiveness of AlloWrap Amniotic Membrane in the reduction of soft tissue swelling in two-level ACDF procedures.

NCT ID: NCT01754649 Completed - Cervical Stenosis Clinical Trials

Use of Misoprostol in Case of Insertion Failure of Intrauterine Contraceptives

Start date: January 2013
Phase: Phase 4
Study type: Interventional

To assess the usefulnes sof misoprostol versus placebo (in a double-blind placebo controlled randomized clinical trial)to facilitate the insertion of copper-IUD and the levonorgestrel-releasing intrauterine system (LNG-IUS) in cases of failure due to cervical stenosis in either nulligravidas and parous women. Additionally to evaluate the side-effects of the misoprostol. The hypothesis is that misoprostol may be better than placebo.

NCT ID: NCT01607775 Completed - Clinical trials for Cervical Disc Degeneration

In-house Produced PMMA- Versus PEEK-cages

Palcage
Start date: February 2009
Phase: Phase 1/Phase 2
Study type: Interventional

Subsidence of cervical cages is a common problem. For the study, a new polyacrylmethacrylate cage was designed and prospectively implanted in patients with a mono- or bilevel cervical pathology. As control, a commercially available PEEK-cage was used, patients were randomized using minimization randomization, controlling for age and bone mineral densitiy. The investigators hypothesize that the newly developed cage has similar clinical and radiological qualities compared to the PEEK-cage, but at a much more favourable cost-performance ratio.