Lung Function Tests in Adolescents With Anorexia Nervosa
Recruitment status was Recruiting
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Purpose
The investigators hypothesize that lung function would be adversely affected at the hypocaloric stage of adolescents suffering from anorexia nervosa.
| Condition |
|---|
|
Anorexia Nervosa |
| Study Type: | Observational |
| Study Design: | Observational Model: Cohort Time Perspective: Prospective |
| Official Title: | Lung Function Tests in Adolescents With Anorexia Nervosa |
- Lung function tests at admission of adolescents with anorexia nervosa [ Time Frame: On addmission to the pediatric ward ] [ Designated as safety issue: No ]
- Lung function tests at discharge of adolescents with anorexia nervosa [ Time Frame: On discharge from the pediatric ward ] [ Designated as safety issue: No ]
| Estimated Enrollment: | 15 |
| Study Start Date: | September 2008 |
| Estimated Study Completion Date: | December 2009 |
| Groups/Cohorts |
|---|
|
Adolescents hospitalized for anorexia nervosa
Adolescent 12-18 years old, fulfilling the DSM IV criteria for anorexia nervosa, hospitalized for medical stabilization and/ or initiation of refeeding
|
|
Controls
Adolescents 12-18 years old without anorexia nervosa hospitalized for reasons other than those involving the respiratory system and with no underlying lung disease
|
Detailed Description:
Anorexia Nervosa in adolescents holds adverse effects on different body systems as the cardiovascular, central nervous, endocrine, bone and gastrointestinal systems. There is paucity of information regarding the adverse effects of this tenacious illness on the lungs of adolescents at the hypocaloric stage of their illness. Based on previous clinical observations we postulate that lung function tests would be adversely effected by the hypocaloric nutrition of adolescents with anorexia nervosa and that they may improve during short refeeding in an inpatient setting of a general pediatric ward. To examine our hypothesis we would check lung function by various parameters of adolescents suffering from AN and a control group of adolescents.
Eligibility| Ages Eligible for Study: | 12 Years to 18 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
| Sampling Method: | Non-Probability Sample |
Adolescents 12-18 years old hospitalized to a pediatric ward
Inclusion Criteria:
- Adolescents with anorexia nervosa
- Ability to preform lung function tests
- Parents signing informed concent and adolescents signing informed ascent
Exclusion Criteria:
- A history of a lung disease
- Intercurrent lung illness
Contacts and Locations| Israel | |
| Bnai Zion Medical Centre, Department of Pediatrics | Recruiting |
| Haifa, Israel, 31048 | |
| Contact: Nogah C Kerem, MD 972-4-8359662 nogah.kerem@b-zion.org.il | |
| Contact: Amir Kugelman, MD 972-4-8359559 dramir@netvision.net.il | |
| Principal Investigator: Nogah C Kerem, MD | |
More Information
No publications provided
| Responsible Party: | Nogah Kerem, Bnai Zion Medical Centre |
| ClinicalTrials.gov Identifier: | NCT00942929 History of Changes |
| Other Study ID Numbers: | 48/08 |
| Study First Received: | July 20, 2009 |
| Last Updated: | July 20, 2009 |
| Health Authority: | Israel: Ministry of Health |
Keywords provided by Bnai Zion Medical Center:
|
anorexia nervosa adolescents lung function tests refeeding |
Additional relevant MeSH terms:
|
Anorexia Anorexia Nervosa Signs and Symptoms, Digestive |
Signs and Symptoms Eating Disorders Mental Disorders |
ClinicalTrials.gov processed this record on May 23, 2013