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Wounds and Injuries clinical trials

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NCT ID: NCT05331118 Recruiting - Delirium Clinical Trials

Perioperative Longitudinal Study of Complications and Long-term Outcomes

PLUTO
Start date: February 21, 2020
Phase:
Study type: Observational [Patient Registry]

Purpose: with an increased risk of complications. Improved preoperative risk stratification and earlier diagnosis of these complications may ameliorate postoperative recovery and improve long-term outcomes. The perioperative longitudinal study of complications and long-term outcomes (PLUTO) aims to establish a comprehensive biorepository that will facilitate research in this field. Patients undergoing elective intermediate to high-risk non-cardiac surgery are eligible for enrolment. For the first 7 postoperative days (or longer as indicated), participants will be subjected to daily bedside visits by dedicated observers, who adjudicate clinical events and perform non-invasive physiological measurements (including handheld spirometry and single-channel EEG). In addition, we will collect blood samples as well as microbiome specimens at selected time points. Primary study outcomes are the postoperative occurrence of nosocomial infections, major adverse cardiac events, pulmonary complications, acute kidney injury and delirium. Secondary outcomes include mortality as well as long-term psychopathology, cognitive dysfunction, and quality of life. PLUTO is the first perioperative biobank worldwide that includes a broad range of high-risk surgical patients, collecting prospective bedside data as well as both blood and microbiome specimens during the entire perioperative period. The data and materials collected in PLUTO will be used to develop, externally validate, and update prognostic prediction models for improved risk assessment, to test novel biomarkers for early detection of postoperative complications and to study the aetiology, attributable morbidity and mortality related to these events.

NCT ID: NCT05330767 Recruiting - Wound of Skin Clinical Trials

DermaClose DUKE Fasciotomy and Wound Study

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

To evaluate the clinical performance of DermaClose and DermaClose XL Continuous External Tissue Expander (CETE) devices to reduce wound size and/or assist with closure in acute full thickness wounds of the skin and assess the need for skin grafting for patients undergoing a four-compartment leg fasciotomy.

NCT ID: NCT05330351 Recruiting - Aspiration Clinical Trials

Gastric Ultrasound in Pediatric Trauma Patients

Start date: March 26, 2022
Phase:
Study type: Observational

Gastric ultrasound has become increasingly utilized to examine volume and quality of gastric contents in the preoperative setting to guide anesthetic management and relay risk of aspiration in both adult and pediatric medicine. Gastric fluid volumes in trauma patients are thought to be elevated due to delayed gastric emptying in the setting of an over-attenuated sympathetic response to physical pain and stress, opioid analgesia, and other associated injuries (traumatic brain). However, there is a paucity of literature examining gastric fluid volumes (GFV), measured by gastric ultrasound, in the pediatric trauma population. The purpose of the study is to assess whether preoperative gastric ultrasound is an accurate method to identify pediatric trauma patients who have elevated GFV (>0.8mL/kg) and high-risk gastric contents (solids, complex liquids, in addition to large volumes).

NCT ID: NCT05328986 Active, not recruiting - COVID-19 Clinical Trials

Kidney Disease After COVID-19

Start date: January 4, 2020
Phase:
Study type: Observational [Patient Registry]

To understand the long-term epidemiology, develop effective risk-prediction and stratification tools, and understand the pathobiology of kidney disease in COVID-19 survivors.

NCT ID: NCT05328674 Recruiting - Knee Injuries Clinical Trials

Clinical and Comparative Evaluation of the Treatment Results of Arthroscopic Reconstruction of Cartilage Defects in the Knee Joint With the Use of Autogenous Cartilage Graft With PRP GF (Platelet-rich Plasma With Growth Factors)

Start date: June 22, 2021
Phase: N/A
Study type: Interventional

Clinical and comparative evaluation of the treatment results of arthroscopic reconstruction of cartilage defects in the knee joint with the use of autogenous cartilage graft with PRP GF (platelet-rich plasma with growth factors)

NCT ID: NCT05328544 Recruiting - Clinical trials for Anterior Cruciate Ligament Injuries

Reconstruction of the Anterior Cruciate Ligament of the Knee Joint, by the Method of Stabilization of the Screw With a Bioabsorbable Method, With or Without the Use of Autogenous Spongiform Bone Grafts.

Start date: August 13, 2021
Phase: N/A
Study type: Interventional

Clinical and comparative evaluation of the results of autograft healing of the tendon of the semitendinus muscle in the tibial canal, after reconstruction of the anterior cruciate ligament of the knee joint, by the method of stabilization of the screw with a bioabsorbable method, with or without the use of autogenous spongiform bone grafts.

NCT ID: NCT05327829 Not yet recruiting - Clinical trials for TBI (Traumatic Brain Injury)

Stimulating After Recovery From Traumatic Brain Injury

SMART
Start date: June 30, 2024
Phase: Early Phase 1
Study type: Interventional

This is a preliminary, prospective interventional study to investigate the feasibility of using transcutaneous alternating current stimulation (TACS) and transcutaneous noninvasive vagal nerve stimulation (tnVNS) after a traumatic brain injury (TBI) to improve cognitive function and decision-making.

NCT ID: NCT05326555 Recruiting - Concussion, Brain Clinical Trials

Dynamic Vision Testing and Concussion Management Dream Team 65

Start date: October 1, 2021
Phase:
Study type: Observational

The purpose of this study is to determine the value of including dynamic vision testing into California State University, Northridge (CSUN) Athletics' established concussion protocol. The study's hypotheses are 1) dynamic vision testing will reveal vision impairments right after a person sustains a concussion, 2) these impairments may still be present upon clearance to return to play.

NCT ID: NCT05326022 Not yet recruiting - Clinical trials for Wound Healing Delayed

Microcurrent Therapy and Low-Level Laser Therapy on Wound Healing

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

The study aiming to compare between the Microcurrent and Low-Level Laser Therapy on wound healing

NCT ID: NCT05325944 Not yet recruiting - Depression Clinical Trials

Digital Mental Health Intervention for Nonsuicidal Self-Injury in Young Adults

Start date: April 1, 2024
Phase: N/A
Study type: Interventional

This is a feasibility trial of a digital mental health intervention aimed at young adults (ages 18-25) with nonsuicidal self-injury and who are not currently engaged in mental health treatment. We will pilot three arms: a self-guided DMHI, the DMHI with low-intensity coaching, or an active control which will involve the delivery of non-interactive psychoeducational content via the same app interface. The primary goals of this project are to evaluate the feasibility of the intervention and trial procedures in preparation for a fully-powered randomized-controlled trial.