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Wounds and Injuries clinical trials

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NCT ID: NCT04386174 Recruiting - Spinal Cord Injury Clinical Trials

Brain Activity in People With Chronic Neuropathic Pain and Spinal Cord Injury

Start date: August 1, 2020
Phase: Early Phase 1
Study type: Interventional

The purpose of this research study is to learn more about how patterns of brain activity change during different thinking tasks and how these changes relate to the intensity and unpleasantness of the neuropathic pain that people with SCI experience.

NCT ID: NCT04373512 Recruiting - Clinical trials for Spinal Cord Injuries

Intravesical Lactobacillus to Reduce Urinary Symptoms After Spinal Cord Injury

Start date: May 20, 2020
Phase: Phase 2
Study type: Interventional

The objectives of the proposed research among this population are: 1) to define clinically meaningful change (i.e. differentiating states of health and illness) with respect to urinary symptoms, urine inflammation, cultivable bacteria, and the urine ecosystem; and 2) to determine the optimal intravesical Lactobacillus RhamnosusGG (LGG®) dose to be used to reduce urinary symptoms in a future clinical trial.

NCT ID: NCT04372797 Recruiting - Clinical trials for Mild Traumatic Brain Injury

Standardized Instruments to Provide Diagnostic and Prognostic Information in Mild Traumatic Brain Injury (mTBI)

Start date: September 30, 2020
Phase: N/A
Study type: Interventional

This study will establish the capability of a suite of conventional tests and the Neurolign Dx_100 I-PAS goggle system to reliably and objectively detect mTBI in an acute setting when comparing individuals with mTBI to controls with minor injuries in a similarly stressful environment.

NCT ID: NCT04372212 Recruiting - Recurrent Hernia Clinical Trials

Needlescopic Inversion and Snaring Versus Ligation of Hernia Sac in Girls

Start date: March 21, 2020
Phase: N/A
Study type: Interventional

Failure of closure of the processus vaginalis during intrauterine life will result in congenital inguinal hernia [CIH]. Exact incidence of CIH in children is not known but it has been reported between 1-5 %. In premature babies, the incidence may reach up to 15-30%. Congenital inguinal hernia is more common in boys than girls, ranging from 4:1 to 10:1 [1]. Although the open inguinal herniotomy and high ligation of the sac is the gold standard line of the treatment, Laparoscopic inguinal hernia repair become a good option. The laparoscopy has many advantages that it is simple, feasible, and safe with detection of the contralateral hernia and other hernias. In addition to laparoscopy results in excellent cosmetic results low wound infection, less pain, and short hospital stay. The non-division of the hernia sac in during laparoscopic hernia repair may be the cause of recurrence and postoperative hydrocele [5]. Division of hernia sac and suturing of proximal part at IIR; is modification of the laparoscopic technique which mimic what happen during open herniotomy. Some authors resected the processus vaginalis and closed the inguinal ring for the repair of CIH. They claimed that they have excellent results with low recurrence.One author described a technique based on the theory that CIH is due to a patent processus vaginalis, and therefore, the procedure should be to entirely resect it, with or without closure of the internal ring. This allows the peritoneal scar tissue to close the area of the ring. Also, this scarring occurs in the extent of the inguinal canal where the dissection took place, therefore causing the same peritoneal scarring and sealing of the inguinal floor with complete resolution of the problem. However, a few studies address the superiority of technique over the other and to date there is no controlled randomized study to compare needlescopic disconnection of the hernia sac and closure of the peritoneum at IIR versus disconnection without closure of the peritoneum.

NCT ID: NCT04371120 Recruiting - Clinical trials for Traumatic Brain Injury

Brain Injury Self-Efficacy Scale Validation

BICSQ
Start date: April 1, 2019
Phase:
Study type: Observational

The purpose of this study is to validate the Brain Injury Self-Efficacy Scale as a measure of self-efficacy in brain injury by comparing it with other measures of self-efficacy, the GSE, and PROMIS self-efficacy.

NCT ID: NCT04368117 Recruiting - Burn Injury Clinical Trials

STAT: Standard Therapy Plus Active Therapy

STAT
Start date: October 26, 2020
Phase: N/A
Study type: Interventional

The objective of the study is to assess the efficacy of STAT, an activity-based therapy protocol compared to standard therapy (ST) to improve functional outcome and reduce disability in patients recovering from burn injury. This randomized multi-center trial is designed with two parallel treatment groups: STAT and ST. Efficacy of the STAT protocol will be determined through comparison to the ST only group. It will be conducted at seven burn centers.

NCT ID: NCT04350359 Recruiting - Clinical trials for Spinal Cord Injuries

Transcutaneous Tibial Nerve Stimulation for Spinal Cord Injury Neurogenic Bladder

TTNS1yr
Start date: June 8, 2020
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if electric stimulation to the leg, called transcutaneous tibial nerve stimulation (TTNS), can improve bladder outcomes in acute spinal cord injury.

NCT ID: NCT04349852 Recruiting - Clinical trials for Traumatic Brain Injury

Verbal Working Memory and Attention Remediation for Adults With Traumatic Brain Injury.

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

This project will examine if computerized cognitive remediation will improve working memory and attention in 25 adults with a mild, moderate, or severe brain injury and compare their cognitive performance to the control group of 25 adults with a mild, moderate, or severe brain injury. The control group will train on computerized tasks of social awareness. Participants in both groups will be assessed prior to training and immediately post-training and one month-post training.

NCT ID: NCT04348253 Recruiting - Ligament Injury Clinical Trials

Danish Multicenter Scapholunate Ligament Study

Start date: August 1, 2018
Phase: N/A
Study type: Interventional

Comparison of two surgical techniques commonly used for reconstruction of the scapholunate (SL) ligament. A randomized multicenter study.

NCT ID: NCT04341038 Recruiting - COVID-19 Clinical Trials

Clinical Trial to Evaluate Methylprednisolone Pulses and Tacrolimus in Patients With COVID-19 Lung Injury

TACROVID
Start date: April 1, 2020
Phase: Phase 3
Study type: Interventional

The primary objective of the study is to evaluate the days until reaching clinical stability after starting randomization in hospitalized patients with elevated inflammatory parameters and severe COVID-19 lung injury.