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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04016207
Other study ID # IIR-DEU-002258
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date April 1, 2020
Est. completion date June 2021

Study information

Verified date April 2020
Source Technische Universität Dresden
Contact Robert Waltereit, MD
Phone +493514582244
Email robert.waltereit@uniklinikum-dresden.de
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Early onset, high prevalence and persistence, as well as developmental comorbidity make affective dysregulation (AD) in childhood one of the most psychosocially impairing and cost-intensive mental conditions. Despite continuous research, there is still a substantial need for optimization of individual treatment strategies in order to improve outcomes and to reduce subjective and economic burden. Here we want to study the change of psychopathological markers of affective dysregulation (AD) treatment of affective dysregulation (AD) in children with Attention Deficit Hyperactivity Disorder (ADHD) treated by Guanfacine. These children did not respond to methylphenidate treatment. The results will allow the generation of a hypothesis for a randomized clinical trial to investigate the efficacy and safety of Guanfacine for the treatment of AD in children.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 40
Est. completion date June 2021
Est. primary completion date March 2021
Accepts healthy volunteers No
Gender All
Age group 6 Years to 17 Years
Eligibility Inclusion Criteria:

- male and female patients (aged 6 to 17 years)

- clinical diagnosis of ADHD (F90.0) or comorbid ADHD and Oppositional defiant disorder (ODD) (F90.1)

- patients with ADHD who did not respond to stimulants

- DADYS is an instrument to assess AD and has a domain for disruptive behaviors. Inclusion criterion for the study is a score of at least moderate (middle) severity in the DADYS parents version this domain

- IQ must be at least 70

- Patients receiving or intended to receive Guanfacin

- Written informed consent by the custodian and the children

Exclusion Criteria:

- unipolar depression, bipolar disorder, schizophrenia or any other psychotic disorder

- current substance abuse

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Guanfacine
regular treatment

Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
Technische Universität Dresden Prof. Dr. Veit Roessner and PD Dr. Robert Waltereit jointly lead and conduct the study

Outcome

Type Measure Description Time frame Safety issue
Primary DADYS-EF (Diagnostikum für Affektive Dysregulation, Eltern-Fragebogen) The DADYS is a German instrument to assess affective dysregulation. The Eltern-Fragebogen is the parents' version of the rating scale. 9 weeks
Secondary DADYS-KF (Diagnostikum für Affektive Dysregulation, Kinder-Fragebogen) The DADYS is a German instrument to assess affective dysregulation. The Kinder-Fragebogen is the childrens' version of the rating scale. 9 weeks
Secondary Conners3L The Conners 3rd Edition™ (Conners 3®) is a thorough assessment of attention-deficit/hyperactivity disorder (ADHD) and its most common comorbid problems and disorders in children and adolescents aged 6 to 18 years. It is a multi-informant assessment that takes into account home, social, and school settings, with rating forms for parents, teachers, and youth. 9 weeks