CLONICEL (Clonidine HCl sustained release)
DrugFlexible Dose (0.1 - 0.4 mg)
NCT Number: NCT00641329
The purpose of this study is to determine if CLONICEL (clonidine HCl sustained release) is a safe and effective add-on to psychostimulant therapy in children and adolescents with attention deficit hyperactivity disorder (ADHD).
Looking for future studies?
Notify Me6 year–17 year
All sexes
Interventional
Phase 3
Little Rock, Arkansas, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Flexible Dose (0.1 - 0.4 mg)
Matching placebo tablets
Time frame: Week 5
Time frame: Throughout Treatment and Follow-up Period
Looking for future studies?
Notify MeAddrenex Pharmaceuticals, Inc.
Industry
Phase III Evaluation of the Safety and Efficacy of CLONICEL (Clonidine HCl Sustained Release) as Add-on to Psychostimulant Medication vs. Psychostimulant Medication Alone in Children and Adolescents With ADHD
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT07836244
ADHD, Attention Deficit Disorder with Hyperactivity
Xi'an, Shaanxi, China
View Trial DetailsNCT04240756
ADHD, Attention Deficit Disorder with Hyperactivity
College Park, Maryland, United States
View Trial DetailsNCT03333668
ADHD, Attention Deficit Disorder with Hyperactivity
London, United Kingdom
View Trial DetailsNCT06626750
ADHD, Attention Deficit Disorder with Hyperactivity
Miami, Florida, United States
View Trial Details