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PROspective Longitudinal All-comer Inclusion Study in Eating Disorders

NCT03224091 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 1000

Last updated 2022-04-07

No results posted yet for this study

Summary

The PROLED study is a prospective and longitudinal study of patients with Eating Disorders. Annual interviews and collection of biological samples are done, as well as during changes in disease course e.g. during hospitalization. Included are qualitative interviews, psychometric tests, questionnaires which are used to collect data on psychopathology. There is also collection of blood, urine and faeces.

Conditions

  • Anorexia Nervosa
  • Bulimia Nervosa
  • Binge-Eating Disorder
  • Eating Disorder NOS

Sponsors & Collaborators

  • University of Southern Denmark

    collaborator OTHER

  • University of Copenhagen

    collaborator OTHER

  • Statens Serum Institut

    collaborator OTHER

  • Mental Health Services in the Capital Region, Denmark

    lead OTHER

Principal Investigators

  • Louise Behrend_Rasmussen, MD,PhD · Mental Health Center Ballerup

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2016-01-25
Primary Completion
2030-04-01
Completion
2030-04-01

Countries

  • Denmark

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03224091 on ClinicalTrials.gov