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Migraine clinical trials

View clinical trials related to Migraine.

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NCT ID: NCT00111722 Completed - Migraine Clinical Trials

Study to Test a Marketed Drug in the Treatment of Menstrual Migraine (0462-072)

Start date: May 27, 2005
Phase: Phase 3
Study type: Interventional

The purpose of this study is to test the effectiveness of a marketed drug in the treatment of a menstrual migraine attack.

NCT ID: NCT00111709 Completed - Migraine Clinical Trials

Study to Test a Marketed Drug in the Treatment of Menstrual Migraine (0462-071)

Start date: May 27, 2005
Phase: Phase 3
Study type: Interventional

The purpose of this study is to test the effectiveness of a marketed drug in the treatment of a menstrual migraine attack.

NCT ID: NCT00095004 Completed - Migraine Clinical Trials

Study to Test an Approved Product in the Early Treatment of Migraine (0462-066)

Start date: October 21, 2004
Phase: Phase 3
Study type: Interventional

The purpose of this study is to test the effectiveness of an approved drug in the early treatment of migraine.

NCT ID: NCT00092963 Completed - Migraine Clinical Trials

Study to Test an Approved Product in the Early Treatment of Migraine (0462-065)

Start date: August 17, 2004
Phase: Phase 3
Study type: Interventional

The purpose of this study is to test the effectiveness of an approved drug in the early treatment of migraine while the pain is still mild.

NCT ID: NCT00071786 Recruiting - Migraine Clinical Trials

Family Study of Affective and Anxiety Spectrum Disorders

Start date: May 21, 2004
Phase:
Study type: Observational

This study will examine how depression, anxiety, and migraine run in families. It will help in defining the risk factors for physical, mental, and health problems-as well as define ways that those problems may be prevented and treated. A broad range of ages among family members will be included to evaluate the patterns of how these disorders are expressed throughout people's lives. Children of all ages will be included, and those ages 8 to 17 will be interviewed directly. Assessments will be collected through criteria of the Diagnostic and Statistical Manual of Mental Disorders IV as well as the spectrum, or range, of mood disorders and co-existing conditions. A member of the study team will visit the participants at home or will do an interview by telephone. Participation will take approximately 3 to 4 hours. Children will complete questionnaires given by the research team as well as questionnaires that they will do by themselves. The questions will pertain to the children's health, including physical and mental health and medical history, social relationships, problems, skills, and ways of dealing with important or stressful issues in their lives. These questionnaires will take up to 1 hour to complete. Health history gathered from adult participants will pertain to height, weight, exercise, and general function. Women will be asked about the use of oral contraceptives, estrogen, and progesterone. In addition, there will be questionnaires on personality and temperamental traits, that is, behavior and impulsiveness. Questions will also involve social intuition, family and other environmental factors, general functioning, and basic demographics such as ethnicity, race, socioeconomic status, marital status, education level, and employment history. Families enrolled in this phase of the research will be invited to participate in the next phase. There would be follow-up to evaluate the development of mood disorders, subtypes, and syndromes across the lifespan.

NCT ID: NCT00060619 Recruiting - Migraine Clinical Trials

Migraine and Recurrent Abdominal Pain in Children

Start date: May 1999
Phase: N/A
Study type: Interventional

This study will evaluate a new model for assessing and treating migraine and recurrent abdominal pain in children. The model combines behavioral techniques such as relaxation training with biologic components such as thermal biofeedback.

NCT ID: NCT00018811 Completed - Migraine Clinical Trials

Psychological Assessment and Treatment of Chronic Benign Headache

Start date: April 1999
Phase: N/A
Study type: Interventional

Subjects with chronic migraine or tension headaches will receive 12 sessions of biofeedback or relaxation training after fulfilling screening, intake interviews, & psychological testing requirements. They will chart headache pain, anger level, & medication usage throughout baseline, treatment, and 3 month follow-up periods. Migraine sufferers will receive a combination of progressive muscle relaxation training and thermal biofeedback (learning to warm hands). Subjects are randomly assigned to receive treatment either in the office with the therapist or from another room (where communication will be over a computer). The research is designed to compare the effectiveness of treatment based on location. Tension headache sufferers will receive training in how to reduce their muscle tension levels. They will be randomly assigned to have equipment monitor muscle tension levels either in the forehead or shoulder regions. The research is designed to compare the effectiveness of feedback to the forehead versus the shoulder muscles.