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Aggression clinical trials

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NCT ID: NCT00554164 Completed - Clinical trials for Lymphoma, High-grade

Positron Emission Tomography Guided Therapy of Aggressive Non-Hodgkin's Lymphomas

PETAL
Start date: November 2007
Phase: Phase 3
Study type: Interventional

The main purpose of the PETAL trial is to determine whether patients with aggressive non-Hodgkin's lymphomas with a persistently positive PET scan after two cycles of chemotherapy benefit from a change of the treatment protocol.

NCT ID: NCT00550147 Completed - Clinical trials for Attention Deficit Disorder With Hyperactivity

Quetiapine and Concerta in the Treatment for ADHD and Aggressive Behavior.

Start date: February 2004
Phase: Phase 2
Study type: Interventional

The primary purpose of this thirteen-week, open-label study is to test the hypothesis that quetiapine in combination with Oros methylphenidate will reduce aggressive symptoms in children and adolescents who have shown inadequate response to OROS methylphenidate alone.

NCT ID: NCT00521560 Completed - Clinical trials for Primary Non-Hodgkin-Lymphoma

A Study of Zevalin and Simultaneous Application of BEAM High-dose Chemotherapy Followed by Autologous Stem Cell Transplantation in Refractory and Relapsed Aggressive Non-Hodgkin Lymphomas

escZ-BEAM
Start date: March 2006
Phase: Phase 2
Study type: Interventional

Phase II Study Concomitant High-Dose Radio-Immuno- and Chemotherapy with simultaneous application of Zevalin and BEAM followed by autologous peripheral stem cell transplantation in relapsed and refractory CD 20+ Non-Hodgkin's lymphoma

NCT ID: NCT00510094 Completed - Aggression Clinical Trials

Effectiveness of Treatment for Relational Aggression in Urban African American Girls

Start date: October 2007
Phase: Phase 3
Study type: Interventional

This study will evaluate the effectiveness of a school-based social cognitive group treatment in reducing aggression (bullying) among relationally aggressive urban African American girls.

NCT ID: NCT00468130 Completed - Autism Clinical Trials

Efficacy of Aripiprazole Versus Placebo in the Reduction of Aggressive and Aberrant Behavior in Autistic Children

Abilify
Start date: May 2006
Phase: N/A
Study type: Interventional

Hypothesis: (1) Aripiprazole treatment will be superior to placebo in reducing aggression and irritability in autistic individuals as shown by reductions in the Aberrant Behavior Checklist-irritability subscale. (2) Aripiprazole treatment will be superior to placebo in the acute treatment of global autism severity. The purpose of this study is to examine the possible benefit of the medication Aripiprazole in autistic individuals.

NCT ID: NCT00467038 Completed - Clinical trials for Borderline Personality Disorder

Treatment of Aggression, Anger and Emotional Dysregulation in Borderline Personality Disorder

Start date: November 2006
Phase: N/A
Study type: Interventional

This study examines the effects of 12 months of dialectical behavior therapy (DBT) for subjects with borderline personality disorder on aggression, anger and emotional dysregulation. Treatment effects will be measured by changes in interview, self-report, psychophysiology testing and fMRI neuroimaging.

NCT ID: NCT00455234 Completed - Psychotic Disorders Clinical Trials

Rapid Tranquillization Trial: TREC-India II

TRECIndia-II
Start date: September 2005
Phase: Phase 3
Study type: Interventional

Three hundred consecutive adult patients presenting to the emergency services of the department of psychiatry and who are diagnosed by the treating doctor to be needing tranquillization to control agitated or aggressive behavior will be randomized to receive either Injection Olanzepine I.M. or Injection Haloperidol 10mg + Injection Promethazine 50 mg in this parallel group, block randomized, centrally-randomzed, allocation-concealed, assessor-blinded pragmatic clinical trial. The main outcome measure that the two treatments would be compared on would be the clinical state of the patient 4 hours after intervention, but the rate of tranquillization, degree of sedation, proportions tranquil and / or asleep at 15, 30, 60 and 240 minutes, need for additional medication, use of physical restraints, doctors called back, numbers absconding and adverse effects at each of these time points would also be compared. Compliance with oral medication and adverse effects at the end of 2 weeks would also be compared.

NCT ID: NCT00444197 Completed - Aggression Clinical Trials

Community-Based Violence Prevention for High-Risk Youth

Start date: August 2001
Phase: Phase 2
Study type: Interventional

Study Aims: 1) Assess the receptiveness of youth and families to injury prevention interventions initiated from the emergency department; 2) In a sample of high risk youth presenting to the ED with interpersonal assault injuries, determine the effectiveness of a home-based family intervention with community linkage compared to a control group.

NCT ID: NCT00431470 Completed - Aggression Clinical Trials

Are Character Building Lessons Effective in Decreasing Bullying Behaviors?

Start date: February 2007
Phase: N/A
Study type: Interventional

Through the use of an educational intervention, the object of this study is to reduce the prevalence of bullying behaviors among fifth grade school age children. Bullying behaviors promote an environment of violence , fear, and hostility. The study will arrange to present six character education lessons in the classroom of fifth grade students in a New York City public school. Questionnaires will be administered to the students before and after all the lessons have been completed. Questionnaires will collect information about the students self perception of their levels of misconduct, impulsivity, confidence, value of non violence, ways of handling anger, opinions of their leadership behaviors, prevalence of bullying behaviors, and indications of levels of self esteem. Also, their fifth grade teachers will complete pre and post treatment student behavioral questionnaires.

NCT ID: NCT00421070 Completed - Clinical trials for Psychiatric &or Mood Disorder

Effect of Massage Therapy on Aggression in a Psychiatric Inpatient Unit

Start date: May 2006
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate whether relaxation massage therapy is effective in reducing the levels of arousal and aggression on a young adult inpatient unit. It is hypothesised that relaxation massage therapy will lead to a lower incidence of violence and aggression on the ward via a reduction in the level of arousal and anxiety among inpatients.