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

H

Hillerod Hospital, Denmark

Status

Unknown

Conditions

Hepatic Injury

Study type

Observational

Funder types

Other

Identifiers

NCT01981213
HIH-2011-17

Details and patient eligibility

About

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.

Enrollment

500 estimated patients

Sex

All

Ages

8 to 18 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 8-18 years-old, who tried to commit suicide with acetaminophen.
  • Children are only included if they have answered all our standard questions.

Exclusion criteria

  • Children with known liver disease prior to the suicide attempt.
  • If a child have several suicide attempts during the inclusion-period, only the 1st will be included.
  • Suicide attempts with other agents than acetaminophen.
  • Children taking medication that enhance the induction of the cytochrome P450 system, increase the production of toxic metabolites, and aggravate the hepatic injury, such as ethanol, rifampin, isoniazid, barbiturates, and carbamazepine, will be excluded.

Trial contacts and locations

1

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Central trial contact

Rikke L. Hedeland, MD

Data sourced from clinicaltrials.gov

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