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Hepatic Injury clinical trials

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NCT ID: NCT06249646 Completed - Liver Injury Clinical Trials

Contained Hepatic Vascular Injuries Following Liver Trauma

Start date: January 1, 2022
Phase:
Study type: Observational

Background: For thirty years, a major shift in the management of liver trauma has been seen. Contained hepatic vascular injuries (CHVI), including pseudo aneurysms and arteriovenous fistula, are often feared due to their risk of secondary bleeding. Nonetheless, knowledge of CHVI is scarce and no guidelines on their management have been set. The investigators aimed to validate the risk factors of CHVI, identify associated morbidities, and establish a management protocol. Study Design: A retrospective study on 318 liver trauma from a level 1 trauma center over the last 15 years, comparing the presence or not of CHVI. Univarious and multivarious analyses were performed. A comparison of the management of CHVI was also performed.

NCT ID: NCT05028595 Completed - Hepatic Injury Clinical Trials

Evaluation of Hepatic Affection in Hemodialysis Patients With Iron Overload in Assiut University Hospital

Start date: January 20, 2019
Phase:
Study type: Observational

Aim of the work 1. Assessment of hepatic affection in patients with ESRD (end stage renal disease) on regular dialysis with iron indices suggesting iron overload. 2. Comparison between HCV -negative HD patients with high and normal TSAT as regard liver iron concentration(LIC) and degree of fibrosis.

NCT ID: NCT01981213 Recruiting - Hepatic Injury Clinical Trials

Attempted Suicide With Acetaminophen Among 8-18 Year-old Children / Adolescents in Denmark

Start date: January 2005
Phase: N/A
Study type: Observational [Patient Registry]

A: Early predictors of hepatic injury after suicide attempt with acetaminophen: To explore the following in a pediatric population with acetaminophen overdose due to suicide attempt: 1) the prevalence of episodes of pre- and in-hospital vomiting and the relationship between the total number of vomiting episodes and hepatic injury, 2) the relevance of the early initiation of N-acetylcysteine (NAC) treatment to hepatic injury, and 3) the presence/absence of illness prior to the suicide attempt and hepatic injury. B: Characteristics, social behaviour, trends and risk factors: 1. To explore the relationship between children admitted to a paediatric department as a result of suicide attempts with acetaminophen and their parents and friends. 2. To determine the extent to which the children had attempted to speak to their parents or other adults about their problems before their suicide attempts. 3. To determine the prevalence of self-mutilation among children with suicidal behaviour. 4. To examine the reasons for these suicide attempts. C: Establishment of the expression of cytochrome P450 in a pediatric including the age-adjusted activities. Urine samples will be analyzed using an HPLC tandem mass spectrometric method, which we have already established in our lab. There will be categorized three groups for comparison: 1. An age-appropriate background population (approximately 200 patients) 2. Paediatric patients that have been admitted to Rigshospitalet, due to severe hepatic injury (approximately 50 patients) 3. Other pediatric patients admitted to their local hospital because of acetaminophen poisoning (approximately 200 patients) A control urine sample will be analyzed three months after the suicide attempt.

NCT ID: NCT01325584 Terminated - Cancer Clinical Trials

Compassionate Use of Omegaven® in the Treatment of Parenteral Nutrition Induced Hepatic Injury

Start date: October 2012
Phase: Phase 2
Study type: Interventional

The purposes of this study are to make Omegaven® available to cancer patients with liver disease and to determine if Omegaven® can improve or prevent further liver disease. The study will also look at the effects Omegaven® has on immune function.