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Spinal Cord Injuries clinical trials

View clinical trials related to Spinal Cord Injuries.

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NCT ID: NCT05513911 Completed - Clinical trials for Spinal Cord Injuries

Intermittent Hypoxia and Upper Extremity EMG Recordings in Individuals With Spinal Cord Injury

Start date: February 3, 2016
Phase: N/A
Study type: Interventional

In this current study, the examiners examine some of the mechanisms of how Acute Intermittent Hypoxia (AIH) effects the upper extremity of survivors of spinal cord injury. This is accomplished both with the use of a load cell to determine elbow strength changes and high density grid electromyography (EMG) to record bicep muscle activations before and after bouts of AIH

NCT ID: NCT05504200 Completed - Clinical trials for Spinal Cord Injuries

Transcutaneous Spinal Cord Stimulation With Bladder and Pelvic Floor Muscle Training

Start date: March 16, 2022
Phase: N/A
Study type: Interventional

Spinal Cord Injury (SCI) disrupts signals between the brain and the rest of the body, this includes signals needed to control the bladder and bowels. Spinal cord stimulation (SCS) (electrical stimulation through electrodes placed on the skin over the spine) has shown potential to improve bladder function. Additionally pelvic floor muscle training (PFMT), has been shown to help control bladder overactivity and reduce incontinence in people with a SCI. This study will investigate PFMT with SCS, and its effects on restoring bladder function, and continence. We aim to recruit 25 participants. Those eligible will be patients from the London Spinal Cord Injury Centre with a supra-sacral SCI (>6 months post-injury), aged 16 years old and above.

NCT ID: NCT05470751 Completed - Multiple Sclerosis Clinical Trials

GentleCath™ for Men Intermittent Catheter With FeelClean™ Technology

Start date: February 2, 2023
Phase:
Study type: Observational

Male self catherterisng observational study.

NCT ID: NCT05425238 Completed - Clinical trials for Cervical Spinal Cord Injury

Blood Flow Restriction Resistance Exercise in Lower Cervical Spinal Cord Injury Patients

Start date: May 15, 2022
Phase: N/A
Study type: Interventional

This study is conducted to investigate the effects of low load Blood Flow Resistance exercise to improve strength and transfer in lower cervical spinal cord injury patientsCervical Spinal Cord injury patients have very less window of opportunity towards functional mode of life. In complete cervical spinal cord injuries only few muscles of upper limb are completely innervated and it is a need to gain maximum output and advantage out of that. Through conventional strength training it is possible to make him do unsupported sitting and transfer But with BFR-RE it may have a possibility to do this procedure in less time than the conventional strength training and patient will save cost of hospital stay as he may timely discharge from hospital early

NCT ID: NCT05411692 Completed - Spinal Cord Injury Clinical Trials

Functional Electrical Stimulations With and Without Motor Priming Exercises in Spinal Cord Injury

Start date: March 15, 2022
Phase: N/A
Study type: Interventional

As functional electrical stimulations has evident role in improving motor control in tenodesis function (power and precision grip) but its results are considered to be short term so addition of task oriented approach i.e. motor priming exercises could enhance the treatment effects . Priming is a mechanism that could easily be a part of a restorative occupational therapy approach, is a therapeutic method with the intent to improve function by targeting underlying neural mechanisms (neuroplasticity and motor control). This will yield the long term effects of priming augmented functional electrical stimulations to enhance the tenodesis function of patients with spinal cord injury. Their combination may produce improvement in hand functions dexterity in spinal cord injury patients.

NCT ID: NCT05406739 Completed - Clinical trials for Spinal Cord Injuries

Feeding Regulation in SCI

Start date: January 5, 2023
Phase: N/A
Study type: Interventional

The overall purpose of this research is to understand the reasons why persons with spinal cord injuries eat more calories than they need to "burn", stay alive, and function. This research will investigate how quickly food moves through a participant's body, the hormones in the participant's body that control energy and digestion, and a participant's impressions of hunger after eating a meal. This will be compared in persons with and without a spinal cord injury.

NCT ID: NCT05406258 Completed - Spinal Cord Injury Clinical Trials

Self-Catheterization Mirror System for Female Patients

Start date: January 11, 2022
Phase: N/A
Study type: Interventional

The purpose of this study is to test a modified mirror system for female patients to use during self-catheterization.

NCT ID: NCT05398913 Completed - Clinical trials for Spinal Cord Injuries

Effects of Rimonabant on Walking Abilities in Incomplete Spinal Cord Injury

RIMOFATSCI-1
Start date: May 12, 2021
Phase: Phase 1/Phase 2
Study type: Interventional

Randomized placebo-controlled safety and feasibility study with crossover design (3 arms). Placebo or Rimonabant 2.5mg or Rimonabant 5mg will be administered for 5 days. Exploratory efficacy will be tested using six-min walking test.

NCT ID: NCT05362422 Completed - Neuropathic Pain Clinical Trials

PAS for Post-SCI Neuropathic Pain

Start date: April 22, 2022
Phase: N/A
Study type: Interventional

The investigators have shown in incomplete SCI patients that long-term paired associative stimulation is capable of restoring voluntary control over some paralyzed muscles and enhancing motor output in the weak muscles. In this study, the investigators will administer long-term paired associative stimulation to patients with incomplete cervical level SCI and SCI- associated neuropathic pain, and investigate its effectiveness for neuropathic pain treatment.

NCT ID: NCT05356442 Completed - Clinical trials for Spinal Cord Injuries

Tenodesis Grip Strength With Functional Hand Recovery in Cervical Spinal Cord Injury

Start date: April 25, 2022
Phase:
Study type: Observational

Spinal cord injury (SCI) is devastating event, the individual become significant burden on their family and society SCI is impairments of sensory, motor and autonomic functions. There is no proper cure and care after SCI, no proper assessment and treatment is present in under developed countries Cross sectional study design will be used and 75 patients included in this study. The population included age 21-55 years, both gender included, teraplegic with lesion level C5-C7, Mini Mental State of Examination ≥24, patient should be medically stable. The patient excluded with history of peripheral nerve lesion as brachial pluxes impairment. For assessment of hand function tools should be used tenodesis grip strength is assessed Graded Redefined Assessment of Strength sensibility and prehension (GRASSP test), and functional hand recovery assessed by jebsen_Taylor Hand function test (JTHFT_IT), hand dynamo meter for grip strength, Action Arm reach test for hand function and spinal cord independence measure will be used. Pearson correlation will be uses to find the association between hand grip strength and functional activities of hand. The collected data will be analyzed by using SPSS 23.