Clinical Trials Logo

Wounds and Injuries clinical trials

View clinical trials related to Wounds and Injuries.

Filter by:

NCT ID: NCT01966237 Completed - Acute Kidney Injury Clinical Trials

Milrinone Pharmacokinetics and Acute Kidney Injury

MIL-PK
Start date: September 2013
Phase:
Study type: Observational

Acute kidney injury (AKI) occurs in 40% of children following heart surgery. Serum creatinine (Scr) is a late biomarker of AKI, rising 24-48 hours after surgery. Thus, for medicines excreted in the urine, AKI could potentially lead to toxic levels in the blood. Urinary biomarkers have the ability to detect AKI earlier. Whether early detection of AKI through urinary biomarkers can predict altered drug levels is unknown. Milrinone is used to improve heart function after surgery, but accumulates in AKI resulting in low blood pressure. Dose adjustments are not currently possible because of the late rise in SCr, and are based on clinical parameters that may lead to clinically relevant over or under-dosing. Thus, this study will address an important knowledge gap being the first to use elevations of AKI biomarker concentrations to anticipate increased milrinone levels.

NCT ID: NCT01956136 Completed - Clinical trials for Traumatic Brain Injury (TBI)

Efficacy and Neural Basis of Music-based Neurological Rehabilitation for Traumatic Brain Injury

MUBI
Start date: March 2014
Phase: N/A
Study type: Interventional

Traumatic brain injury (TBI) is one of the leading causes of serious, life-long disability among adolescents and young adults. Especially the cognitive, emotional, and motors deficits caused by TBI often impair everyday psychosocial functioning, quality of life and ability to work. The purpose of the study is to determine the long-term effect of music-based rehabilitation on cognitive, motor, emotional, and social recovery after TBI in adolescents and young adults, and to study the neural mechanisms that underlie behavioural recovery and the efficacy of music.

NCT ID: NCT01955785 Completed - Clinical trials for Traumatic Brain Injury

Respiratory Treatment of Patients With Moderate and Severe Traumatic Brain Injury

Start date: September 2013
Phase: N/A
Study type: Interventional

Intracranial pressure (ICP) in patients with traumatic brain injury (TBI) is influenced by several factors of which one is arterial CO2 tension. Patient with TBI are often sedated and mechanically ventilated in order to secure a stable PaCO2. This study compares two ventilation modus; Pressure Controlled Ventilation (PC) and Pressure Regulated Volume Controlled ventilation (PRVC) in order to observe which of the two ventilation strategies results in a more stable ICP and arterial CO2 pressure (PaCO2).

NCT ID: NCT01948934 Completed - Wound Clinical Trials

Clinic Trial in Phase 1 Using Amniotic Membrane for the Skin Replacement in Big Wounds

Start date: June 2012
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine the safety of use of a new therapeutic strategy for the treatment of patients with large wounds

NCT ID: NCT01942564 Completed - Head Injury Clinical Trials

The Head Injury-associated Photosensitivity and Pupillary Function (HIPP) Study

HIPP
Start date: August 2013
Phase: N/A
Study type: Observational

After a head injury, many people find that exposure to light causes them increased discomfort. By measuring how the pupil in the eye constricts to flashes of red and blue light, this study will investigate whether this phenomenon is due to a change in the eye's sensitivity to light.

NCT ID: NCT01938222 Completed - Clinical trials for Surgical Wound Infection

Short Stitch Monomax®

Short-Stitch
Start date: January 2013
Phase:
Study type: Observational

A number of studies identifies abdominal hernia as the most frequent postoperative complication following laparotomy with percentages of 9-20% - depending on duration of follow-up. It is based on a multifactorial basis, including factors concerning individual, patient-specific factors, factors related to the operational technique as well as particular surgical factors. Wound complications have been reported by 7-12%, burst abdomen rate (dehiscence) < 5 days being 2-4%, wound infection rate (+/- wound dehiscence) ≥ 5 days being 6-10%. In emergency procedures (e.g. ileus, perforation of hollow organ) a wound complication rate of up to 50 % has to be expected. According to new, first findings from recent studies the rates of wound healing complication and burst abdomen can be reduced significantly. Depending on the study, to almost 50%. The principle is based on the reduction of the stitch length and type of the inserted suture. The stitches are closer and with less distance to the edge of fascia. Due to the much thinner suture it still comes here to a quantitative reduction of the inserted suture. The data collected using the MonoMax® suture in the short stitch technique will be compared to the results of the ISSAAC trial, in which the MonoMax® suture was used in the long stitch suture technique. The generated data are thus subject of retrospective comparison with a historical control group (ISSAAC study).

NCT ID: NCT01936246 Completed - Clinical trials for Hypoxic-ischemic Encephalopathy

Protein Supplementation in Infants With Brain Injury

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

To date, few studies have been done regarding nutrition supplementation in infants with brain injury. Therefore, the investigators are proposing to study the effects of protein supplementation in this group of babies. The investigators will recruit 24 infants with brain injury (evidence of hemorrhage, white matter injury, or gray matter injury) admitted to the Cincinnati Children's Hospital Neonatal Intensive Care Unit (NICU) into the study. Upon diagnosis, the investigators will obtain consent from the parents for participation in the study, then randomly assign the baby to one of two groups - an increased protein group and a control group. Both groups of infants will be monitored to ensure no adverse effects occur due to the supplementation. Protein supplementation will continue for the first 12 months of age. Growth parameters, such as weight, length, and head circumference, will be measured while the infant is the NICU. Head circumference will be measured in the investigators outpatient clinic at three, six, and 12 months of age. At 18-22 months, the infants will be tested for neurodevelopmental outcomes using the Bayley Scales of Infant Development. The investigators hypothesize that infants who receive the additional protein will demonstrate increased head growth and improved neurodevelopmental outcomes.

NCT ID: NCT01935609 Completed - Clinical trials for Traumatic Brain Injury

Evaluation of a Skill-Building, Supportive, and Educational Intervention for Couples

Start date: March 2013
Phase: N/A
Study type: Interventional

1. To evaluate the efficacy of a structured outpatient couples intervention program (Therapeutic Couples Intervention, TCI) on couples' marital quality after acquired brain injury (ABI). 2. To assess the impact of the TCI on the emotional well-being of persons with ABI and their partners. 3. To ascertain the impact of the TCI on caregiver burden and unmet needs as reported by partners of persons with ABI. 4. To examine the extent to which treatment benefits for survivors and their caregiving partners are sustained in the longer-term.

NCT ID: NCT01927003 Completed - Clinical trials for Soft Tissue Injuries

Direct and Reversed Dorsal Digito-metacarpal Flaps: A Review of 24 Cases

Start date: April 2009
Phase: N/A
Study type: Interventional

Multiple digital injuries are often complex and severe, and the commonly used local and regional flaps may not be feasible. The authors reconstruct soft tissue defects of the fingers using the dorsal digito-metacarpal flap and evaluate the efficacy of this technique.

NCT ID: NCT01925963 Completed - Clinical trials for Focus: Healthy Adults Without Brain Injury

Normative Datasets for Assessments Planned for Mild Traumatic Brain Injury (NORMAL)

NORMAL
Start date: January 10, 2014
Phase:
Study type: Observational

The purpose of the research study is to collect information about brain function and structure among active duty military personnel or civilians who are healthy. Researchers want to develop a database from normal volunteers that will be used in comparison with a similar database from active duty military with post-concussive syndrome (PCS) from a mild traumatic brain injury. Findings from this study may be used to design larger studies that will evaluate whether hyperbaric oxygen treatments actually improve PCS. Participants in this study will undergo numerous tests to assess physical, mental, and intellectual health and how they might change over time. Participants will wear heart and activity monitors, undergo brain imaging, provide blood and urine for laboratory testing, and have vision, hearing, balance, and muscle function tests. They will also complete a number of questionnaires and interviews. This battery of tests will be repeated twice more over the course of 6 months.