Genetic Abnormalities and Biological Changes of Panic Disorder Patients After Pharmacotherapy
NCT00515996 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 80
Last updated 2007-08-14
Summary
We plan to examine genetic polymorphism of catechol-O-methyltransferase in panic disorder and neurobiological changes of panic disorder patients after 12 weeks of pharmacotherapy with paroxetine. We plan to include 40 panic disorder patients and 40 normal control subjects in this study for 3 years.
Conditions
- Panic Disorder
Sponsors & Collaborators
-
Samsung Medical Center
lead OTHER
Principal Investigators
-
Bum-Hee Yu, M.D. & Ph.D. · Samsung Medical Center, Sungkyunkwan University School of Medicine
Eligibility
- Min Age
- 20 Years
- Max Age
- 60 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2006-01-31
- Completion
- 2008-12-31
Countries
- South Korea
Study Locations
More Related Trials
-
Costs of Lost Productive Time Among Korean Workers With Panic Disorder and Effect of Treatment With Paroxetine Controlled Release
NCT00492414 ·Status: UNKNOWN ·Phase: PHASE4
-
A 10-Week, Open-Label, Flexible Dose Adaptive Study Evaluating the Efficacy of Vortioxetine in Subjects With Panic Disorder
NCT02395510 ·Status: COMPLETED ·Phase: PHASE4
-
Treatment of Panic Disorder Among Individuals Consulting Emergency Departments for Non Cardiac Chest Pain
NCT00736346 ·Status: UNKNOWN ·Phase: NA
-
Combination of Paroxetine CR and Quetiapine for the Treatment of Refractory Generalized Anxiety Disorder
NCT00113295 ·Status: COMPLETED ·Phase: PHASE4
-
Study Of Generalized Anxiety Disorder
NCT00135525 ·Status: COMPLETED ·Phase: PHASE2
-
Secondary Prevention With Paroxetine vs. Placebo in Subthreshold Posttraumatic Stress Disorder (PTSD)
NCT00560612 ·Status: COMPLETED ·Phase: PHASE4
-
Treatment of Panic Disorder: Long Term Strategies
NCT00000368 ·Status: COMPLETED ·Phase: PHASE3
-
Study Comparing Venlafaxine vs. Paroxetine in Panic Disorder
NCT00195598 ·Status: COMPLETED ·Phase: PHASE3
-
Investigations of Factors Associated With Treatment Response and Prognosis in Anxiety Disorders
NCT06773585 ·Status: NOT_YET_RECRUITING
-
Mechanisms of Panic Disorders Treatment
NCT01323556 ·Status: UNKNOWN ·Phase: PHASE2/PHASE3
-
A 52-Week Open-Label Safety Study of PD 0332334 in Subjects With Generalized Anxiety Disorder (GAD)
NCT00735267 ·Status: TERMINATED ·Phase: PHASE3
-
Expectation of Unpleasant Events in Anxiety Disorders
NCT00055224 ·Status: COMPLETED ·Phase: NA
-
Drug Treatment Validation of Functional Magnetic Resonance Imaging in Generalized Anxiety Disorder
NCT00662259 ·Status: COMPLETED ·Phase: PHASE4
-
A 10-week Study Evaluating the Efficacy and Safety of PD 0332334 in Patients With Generalized Anxiety Disorder (2)
NCT00658372 ·Status: TERMINATED ·Phase: PHASE3
-
A Phase 2b Study of BNC210 Tablet Formulation in Adults With Post-Traumatic Stress Disorder (PTSD)
NCT04951076 ·Status: COMPLETED ·Phase: PHASE2
-
An Eight-Week Study to Evaluate the Efficacy and Safety of SR58611A in Patients With Generalized Anxiety Disorder
NCT00266747 ·Status: COMPLETED ·Phase: PHASE3
-
Clinical Study Assessing a New Scale to Measure Onset of Action in Generalized Anxiety Disorder
NCT00715039 ·Status: COMPLETED ·Phase: NA
-
The Study of the Pathogenesis and Cognitive Behavioral Group Therapy in Obsessive-Compulsive Disorder
NCT02739061 ·Status: COMPLETED ·Phase: NA
-
Threat Reversal Abnormality in Patients With Anxiety Disorders
NCT06232369 ·Status: NOT_YET_RECRUITING ·Phase: NA
-
An Eight-week Study Evaluating the Efficacy and Tolerability of Two Doses of SSR149415 in Outpatients With Generalized Anxiety Disorder
NCT00374166 ·Status: COMPLETED ·Phase: PHASE2
-
An Open-label Study to Investigate the Absorption, Metabolism and Excretion of Radiolabeled PD 0332334 in Six Healthy Male Volunteers
NCT00537615 ·Status: COMPLETED ·Phase: PHASE1
-
Intracranial Neurophysiological Signatures of Fear and Anxiety in Humans
NCT05120635 ·Status: RECRUITING ·Phase: NA
-
Org 25935 Versus Placebo as Augmentation to Cognitive-behavioral Therapy to Treat Panic Disorder (P05705)
NCT00725725 ·Status: TERMINATED ·Phase: PHASE2
-
Special Drug Use Investigation for PAXIL Tablet (Investigation in Case of Administered From 20mg/Day)
NCT01371474 ·Status: COMPLETED
-
An Eight-Week Study to Evaluate the Efficacy and Safety of SR58611A in Patients With Generalized Anxiety Disorder
NCT00332891 ·Status: COMPLETED ·Phase: PHASE3