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NCT ID: NCT00358995 Completed - Clinical trials for Obsessive Compulsive Disorder

A Cognitive Behavioral Therapy of Primary Obsessions in Obsessive Compulsive Disorder

Start date: July 2002
Phase: N/A
Study type: Interventional

A New Cognitive Behavioral Therapy to Target Distorted Appraisals Characteristic of Primary Obsessions in Obsessive Compulsive Disorder

NCT ID: NCT00358657 Terminated - Clinical trials for Severe Aplastic Anemia

Fludarabine Phosphate, Cyclophosphamide, and Total-Body Irradiation Followed by Donor Bone Marrow Transplant and Cyclophosphamide, Mycophenolate Mofetil, Tacrolimus, and Sirolimus in Treating Patients With Primary Immunodeficiency Disorders or Noncancerous Inherited Disorders

Start date: May 24, 2006
Phase: Phase 2
Study type: Interventional

This phase I/II trial studies the side effects of fludarabine phosphate, cyclophosphamide and total-body irradiation followed by donor bone marrow transplant and cyclophosphamide, mycophenolate mofetil, tacrolimus, and sirolimus in treating patients with primary immunodeficiency disorders or noncancerous inherited disorders. Giving low doses of chemotherapy and total-body irradiation before a bone marrow transplant helps prepare the patient's body to accept the incoming donor's bone marrow and decrease the risk that the patient's immune system will reject the donor's stem cells. When the healthy stem cells from a donor are infused into the patient they may help the patient's bone marrow make stem cells, red blood cells, white blood cells, and platelets. Sometimes the transplanted cells from a donor can make an immune response against the body's normal cells called graft versus host disease. Giving cyclophosphamide, mycophenolate mofetil, tacrolimus, and sirolimus after the transplant may help decrease this from happening.

NCT ID: NCT00357006 Completed - Schizophrenia Clinical Trials

A Definitive Estrogen Patch Study (ADEPT)

Start date: July 2006
Phase: Phase 2
Study type: Interventional

OBJECTIVE: To test the use of adjunctive estrogen in a 8 week, three-arm, double-blind, placebo-controlled study in the treatment of psychotic symptoms in women with schizophrenia. HYPOTHESIS: That women receiving adjunctive estrogen will demonstrate significantly greater improvements in the symptoms of schizophrenia than women receiving adjunctive placebo. STUDY POPULATION: 180 women will be recruited over a three-year period across three sites. Participant will be of potential child-bearing age (Pre-menopausal and Post-menarche) with a current diagnosis of Schizophrenia, Schizophreniform Disorder, or Schizoaffective Disorder (not in manic phase)according to the Mini International Neuropsychiatric Interview (MINI). STUDY MEDICATION: Estradiol. One third of the participants (n=60) will be randomised to receive adjunctive 100mcg Estradiol; one third of the participants (n=60) will be randomised to receive adjunctive 200mcg Estradiol n=60; and, one third of the participants (n=60) will be randomised to receive adjunctive placebo n=60). All patches will be covered with identical adhesive contact to ensure the "blind" is maintained. STUDY EVALUATIONS: Data will be collected over a two-month period for each participant. Visits will be performed at baseline, and then at weekly or fortnightly intervals. A total of six visits will be completed for each participant. The following evaluations will be performed: i) Inclusion/exclusion checklist. (Baseline visit only) ii) Informed consent. (Baseline visit only) iii)psychiatric evaluation to determine diagnosis. (Baseline visit only) iv) General clinical evaluation including medical history, current conditions and a non-invasive physical examination, body weight, vital signs. (Baseline and endpoint visits) v) Medication history. (Baseline and evaluation visits) vi) Demographics. (Baseline visits only) vii) The primary outcome measures will be the Positive and Negative Syndrome Scale (PANSS), which will be taken at weeks 1, 2, 4 and 8 of the trial. Cognitive testing will take place at baseline and 8 weeks. Side effects will be assessed at weeks 1, 2, 4, 6, and 8 to measure changes in subject's reported side effects during the trial. viii) Laboratory tests including; Serum levels of mood stabiliser, LH, FSH, Estrogen, Progesterone, Prolactin, DHEA,Testosterone and(Baseline and evaluation visits).

NCT ID: NCT00356070 Completed - Clinical trials for Attention Deficit Hyperactivity Disorder

Treatment of Prisoners With Attention Deficit Hyperactive Disorder in Trondheim Prison

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

The treatment of ADHD in jail will help the prisoners in their rehabilitation process

NCT ID: NCT00355927 Enrolling by invitation - Parkinson Disease Clinical Trials

Sedation During Microelectrode Recordings Before Deep Brain Stimulation for Movement Disorders.

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

The purpose of this study is to detect possible changes in the electrical activity of the Basal Ganglia related to sedation during deep brain stimulation surgery.

NCT ID: NCT00353470 Completed - Anxiety Disorders Clinical Trials

Comparison of Psychotherapy Programs to Treat Panic Disorder

Start date: September 2006
Phase: Phase 3
Study type: Interventional

This study will determine the relative effectiveness of three psychotherapies in treating people with a panic disorder.

NCT ID: NCT00353379 Terminated - Clinical trials for Personality Disorders

Pharmacology of Cognition in Schizotypal Personality Disorder

Start date: September 1995
Phase: Phase 4
Study type: Interventional

This study will determine the effectiveness of guanfacine in improving cognitive and functional impairments in schizotypal personality disorder.

NCT ID: NCT00352469 Completed - Anxiety Disorders Clinical Trials

Trial of Seroquel SR for Alcohol Dependence and Comorbid Anxiety

Start date: February 2006
Phase: Phase 4
Study type: Interventional

Alcohol use disorders (AUDs) are a major problem facing our society. Their treatment is complex, and involves multiple behavioral and pharmacotherapy interventions. There are 3 approved medications for AUDs, but their efficacy for AUDs that co-exist with anxiety disorders is unknown. This study explores the effects of the medication, sustained-release quetiapine fumarate (Seroquel SR) for the treatment of alcohol dependence and co-morbid anxiety. Primary outcome measure is the amount of alcohol used. Secondary outcome measures include craving for alcohol, length of sobriety from drinking and level of anxiety with Seroquel SR.

NCT ID: NCT00349973 Completed - Schizophrenia Clinical Trials

Clinical Trial of Dipyridamole in Schizophrenia

Start date: May 2001
Phase: N/A
Study type: Interventional

This is a 6-week, randomized, double blind, parallel groups designed, olanzapine-controlled trial of oral dipyridamole in symptomatic patients with a (DSM IV) diagnosis of schizophrenia, schizoaffective or schizophreniform disorder. This pilot study aims to provide preliminary estimates of whether the effect sizes of dipyridamole on positive symptoms, negative symptoms, and cognitive deficits differ between schizophrenia patients treated with dipyridamole, and schizophrenia patients treated with olanzapine. A total of 30 subjects will be recruited locally.

NCT ID: NCT00347269 Completed - Clinical trials for Post-traumatic Stress Disorder

Primary Care Intervention Strategy for Anxiety Disorders

Start date: June 2006
Phase: Phase 4
Study type: Interventional

This study will compare the effectiveness of an intervention strategy for the treatment of people with post traumatic stress disorder, generalized anxiety disorder, panic disorder, and social anxiety disorder in the primary care setting.