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Spinal Stenosis clinical trials

View clinical trials related to Spinal Stenosis.

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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: NCT05403775 Recruiting - Clinical trials for Lumbar Spinal Stenosis

Application of 3D Printing Guide Plate in Dorsal Root Ganglion Intervention Treatments

Start date: July 8, 2022
Phase: N/A
Study type: Interventional

This study applies 3D-printed customized guide plate in assisting the accurate puncture in transforaminal epidural steroid injection (TFESI) combined with pulsed radiofrequency (PRF) treatment. This technique can shorten reduce the intra-operative radiation, and do not affect the surgical outcome.

NCT ID: NCT05392361 Completed - Clinical trials for Lumbar Spinal Stenosis With Nocturnal Calf Cramps

Effect of Baclofen Treatment on Nocturnal Muscle Cramps in Patients With Lumbar Spinal Stenosis: a Randomized Clinical Trial

Start date: June 9, 2022
Phase: N/A
Study type: Interventional

Nocturnal calf cramps is a common complaint in patients with lumbar spinal stenosis. The purpose of this study is to evaluate the effect of baclofen in lumbar spinal stenosis patients receiving conservative therapy. We will compare pain score, insomnia severity, functional ability and patient satisfaction between control (conservative management for spinal stenosis) and baclofen group (conservative management for spinal stenosis plus baclofen treatment).

NCT ID: NCT05375201 Recruiting - Clinical trials for Degenerative Disc Disease

Clinical Decision-Making and Virtual Reality Exercise

Start date: January 1, 2021
Phase: N/A
Study type: Interventional

Degenerative lumbar spine disease (DLSD) is common in elderly individuals and can result in pain, muscle weakness, and paresthesia. Numerous studies have reported that patients with DLSD usually have postural balance instability, which may affect the patient's gait, functional activities, and quality of life. The investigators propose to achieve the following aims: (1) to develop a clinical balance diagnostic tool to identify patients with DLSD who may require lumbar surgery (2) to investigate the effects of virtual reality skateboard exercise training on gait and balance in patients with DLSD, as well as to compare them with asymptomatic participants.

NCT ID: NCT05366140 Recruiting - Spinal Stenosis Clinical Trials

Thoracic-Lumbar Arthrodesis- Implanet Jazz

Start date: February 3, 2022
Phase:
Study type: Observational [Patient Registry]

Establish a data repository of patients who have undergone single, two-, or three-level lumbar instrumented arthrodesis procedures supplemented by the Implanet Jazz System.

NCT ID: NCT05345249 Completed - Clinical trials for Lumbar Spinal Stenosis

Erector Spinae Plane Block as Pain Management After Lumbar Fusion Surgery

RCT-ESPB
Start date: June 1, 2022
Phase: Phase 4
Study type: Interventional

Rationale: Lumbar spine surgery is associated with high postoperative pain scores and analgesic use, despite use of multimodal analgesia. The erector spinae plane block (ESPB) is a promising locoregional anesthetic technique for this type of surgery. The literature is not yet conclusive about the effectiveness of this technique on reducing postoperative pain intensity. Objective: The objective of this study is to evaluate the analgesic effect of ESPB as add-on therapy to multimodal analgesia on early postoperative pain intensity after lumbar spinal fusion surgery compared to placebo. Study design: The study is designed as a prospective mono-centre, randomized, double-blinded, placebo-controlled trial. Study population: 76 patients ≥ 18 years of age requiring elective lumbar spinal fusion surgery involving one to four fusion levels. Intervention: Patients will receive ultrasound-guided ESPB with either ropivacaine or placebo at the end of surgery. Main study parameters/endpoints: Main study parameter is pain intensity upon emergence from anesthesia measured with the Numeric Rating Scale. A minimal clinically important difference is considered to be a decrease of 1.5 points. Secondary endpoints are pain intensity during hospital stay and after 30 days, opioid use during hospital stay and after 30 days, opioid side effects, use of anti-emetics, time to first opioid use/request, length of hospital stay, quality of recovery at discharge. Nature and extent of the burden and risks associated with participation, benefit and group relatedness: The Sint Maartenskliniek is experienced in applying locoregional analgesia, the use of ropivacaine and using sonography. The procedure of administering ESPB has a very low risk of complications. Receiving placebo is justifiable because this group will not be withhold standard treatment. The risks of receiving placebo are negligible. The patients will visit the clinic at regular follow-up moments.

NCT ID: NCT05329129 Recruiting - Clinical trials for Degenerative Disc Disease

OssDsign® Spine Registry Study ("Propel")

Start date: March 23, 2022
Phase:
Study type: Observational

The purpose of this multi-center, prospective, observational registry is to gather information on the clinical outcomes and real-world use of commercially available bone graft substitutes manufactured by OssDsign® AB, in patients who require spine fusion.

NCT ID: NCT05315466 Completed - Clinical trials for Lumbar Spinal Stenosis

Comparison Between Surgical and Conservative Treatment for Lumbar Stenosis

Start date: August 8, 2012
Phase: N/A
Study type: Interventional

This study aims to compare the outcomes of surgical treatment and conservative treatment at medium- and long-term period (minimum 2 years) in patients with lumbar stenosis who come to the observation of the PI's Team at the Rizzoli Orthopaedic Institute, through a series exhaustive questionnaires to self-administer to patients in order to define a path of "decision-making" as effective as possible for the patient and the doctor.

NCT ID: NCT05312281 Recruiting - Spinal Stenosis Clinical Trials

Study Comparing Postoperative Treatment After Surgical Decompression for Lumbar Spinal Stenosis.

SURGIMMO
Start date: June 28, 2022
Phase: N/A
Study type: Interventional

The aim of the study is to assess the benefit of wearing a lumbar orthosis after surgery for spinal stenosis. It will be evaluated if a post-surgery immobilization for 6 weeks with a lumbar orthosis reduces early recurrence, increases walking distance, decreases significantly faster pain and pain medication after surgery

NCT ID: NCT05309447 Active, not recruiting - Clinical trials for Lumbar Spinal Stenosis

Effect of Muscle Fatigue on Spinal Imbalance and Motion in Lumbar Spinal Stenosis

MuscLSS
Start date: November 11, 2021
Phase:
Study type: Observational

This study assesses spinal imbalance and motion in patients with sLSS and elicits fatigue via back exercises and compares spinal imbalance and motion before and after the fatigue exercise and compares these to healthy controls, allowing to associate sLSS-specific motion patterns to paraspinal muscle fatigue.