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Wounds and Injuries clinical trials

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NCT ID: NCT04551391 Completed - Acute Kidney Injury Clinical Trials

Kidney Recovery After Acute Kidney Injury - Longitudinal Study

KRAKIL
Start date: January 7, 2020
Phase:
Study type: Observational

The endothelin (ET) system is an active target in human Acute Kidney Injury (AKI). Our primary hypothesis is that the circulating blood concentration of ET will be higher in patients with AKI than in matched controls.

NCT ID: NCT04548479 Completed - Trauma Chest Clinical Trials

A Comparative Study of Incentive Spirometry and Positive Expiratory Pressure in Chest Trauma

Start date: March 3, 2020
Phase: N/A
Study type: Interventional

Chest trauma (CT) patients with 3 or more ribs fractures with or without pleuropulmonary injury are an indicator of severity. Chest physiotherapy (CP) and analgesia is the first line treatment in these patients. The aim study is to evaluate the effect of positive expiratory pressure (PEP) breathing compared to the incentive spirometry in terms of pain control in the recent phase of CT.

NCT ID: NCT04548180 Completed - Clinical trials for Traumatic Brain Injury

Genome-Wide Assocation Study in Patients With Brain Injury Associated Fatigue and Altered Cognition (BIAFAC)

Start date: June 21, 2021
Phase:
Study type: Observational

The aim of this study is elucidate genetic susceptibility of patients with traumatic brain injury (TBI) and symptoms of Brain Injury Associated Fatigue and Altered Cognition (BIAFAC) using genome-wide association study (GWAS).

NCT ID: NCT04537325 Completed - Acute Kidney Injury Clinical Trials

Prevention of Acute Kidney Injury After Transcatheter Aortic Valve Implantation

Start date: January 20, 2017
Phase: N/A
Study type: Interventional

Randomized controlled, single-center trial randomizing patients with chronic kidney disease and symptomatic severe aortic valve stenosis undergoing transcatheter aortic valve implantation (TAVI). Patients are randomized in a 1:1 ratio to periprocedural intravenous hydration matched to urine output using the RenalGuard system and to standard hydration. The purpose of the study is to test, wether the controlled intravenous hydration with the RenalGuard system is superior to standard hydration to prevent acute kidney injury after TAVI.

NCT ID: NCT04536818 Completed - Clinical trials for Penetrating Abdominal Trauma

Outcomes After Laparotomy for Penetrating Abdominal Trauma

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

The purpose of this study is to evaluate outcomes of adult patients hospitalised due to penetrating abdominal trauma at a tertiary trauma hospital in South Africa. Our primary objective is to study the association between waiting time to surgery and outcome (mortality, complications, and length of hospital stay) in normotensive patients treated with laparotomy for penetrating abdominal trauma.

NCT ID: NCT04535635 Completed - Muscle Injury Clinical Trials

Effects of ART® on Lower Limb Myofascial Pain and Function

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

This is a feasibility study to determine if the investigators can conduct a clinical trial with a sham and control soft tissue treatment. The primary research questions are can the investigators provide the treatments as specified, can they recruit a sufficient number of participants, and does ART® decrease pain and improve function in 20-50 year-old adults with subacute or chronic lower limb soft-tissue injuries compared to a sham treatment? This is a pre-post ART® pilot study with a control group that would receive a sham ART® treatment. The study group is 20-50 year-old adults with subacute or chronic lower limb soft tissue injuries.

NCT ID: NCT04525482 Completed - Clinical trials for Brain Injuries, Traumatic

Application of Early Goal-directed Sedation in Patients With Severe Brain Injury

Start date: January 1, 2017
Phase: N/A
Study type: Interventional

EGDS management strategy was implemented in ICU patients with severe brain injury, the depth of sedation and GCS score were monitored, and the protective effects of EGDS strategy and standard sedation strategy on the brain of patients with severe brain injury were discussed.

NCT ID: NCT04518904 Completed - Clinical trials for Pulmonary Contusion , Chest Trauma , Prediction Model

Establishment of a Prognosis Prediction Model and Scoring Criteria of Pulmonary Contusion Caused by Severe Thoracic Trauma

Start date: January 1, 2014
Phase:
Study type: Observational

Pulmonary contusion caused by severe thoracic trauma is a complex disease. Some patients may be secondary to severe complications such as pulmonary infection or even acute respiratory distress syndrome. At present, there have been no reports on related studies based on Chinese population. In this study, 800 patients with pulmonary contusion will be retrospectively investigated to determine the risk factors and independent risk factors of their poor prognosis, and to construct a prognosis prediction model and scoring criteria.

NCT ID: NCT04516148 Completed - Surgery Clinical Trials

A Randomized, Controlled Trial of the Effectiveness of Perioperative Antibiotics for Reduction of Burn Wound Bacterial Concentration Following Grafting

Start date: May 29, 2018
Phase: Phase 4
Study type: Interventional

The purpose of this study if to evaluate the effectiveness of prophylactic antibiotics given during surgery in reducing the concentration of bacteria in a burn wound after surgery.

NCT ID: NCT04514783 Completed - Wound Heal Clinical Trials

Healthy Tissue Preservation During Wound Debridement by Using Debritom+ Micro Water Jet Technology

Debritom
Start date: January 1, 2022
Phase: N/A
Study type: Interventional

Chronic wounds are common and carry out an important and often neglected burden not only to the individual, the family but also to the society as a whole. The therapeutic approach to the management of chronic wounds include wound bed preparation or wound dressing management. Wound bed preparation is a concept emphasizing a holistic and systematic approach to evaluate and remove barriers to the healing process to allow the wound healing process to progress normally. Debridement is an integrated part of wound bed preparation, achieving certain goals and, thus, creating a healthy wound bed, margins and peri-wound skin with the objective to promote and accelerate healing. Debridement is defined as the removal of foreign material and necrotic tissue from a wound and it can also help to stimulate wound healing. However, not all methods of debridement are the same. Each method has advantages and disadvantages that must be clearly understood. In the present clinical practice, there are several methods of wound debridement: autolytic, enzymatic, mechanical, surgical (sharp) and biologic. The most common method is the mechanical debridement. Currently a micro-water jet technique was introduced into clinical practice. The micro-water jet technique Debritom+ is an effective alternative to traditional instrument interventions performed with the scalpel and/or curette. A sterile liquid is expelled from a nozzle at a selected intensity and accurately sprayed onto the wound surface. The desired effect is the generation of targeted micro-bleedings to stimulate regeneration and healing processes while preserving the underlying healthy tissue. Today, there is no clinical evidence quantitatively comparing one debridement method over the other. Therefore the invesitgators propose a pilot study to measure the extent of tissue loss after debridement using Debritom+ micro-water jet technology versus traditional instrument debridement procedure using scalpel and curette.