Baltimore, MD Bulimia Research Study
The Johns Hopkins Eating Disorders Program is seeking women 18-40
years old with bulimia nervosa interested in a research study funded
by the Klarman Family Foundation. The study includes a health
assessment, blood testing, and pictures of the brain taken using a
medical scanner. Eligible women will be paid up to $400 for their
participation and will be offered 6 weeks of outpatient treatment.
Please call (410) 955-3863 for more information.
PI: Angela Guarda, MD
Clinics and Hospitals Team up to Study Eating Disorders: Six
North American sites are teaming up to evaluate outpatient
treatments for adolescents with anorexia nervosa.
To date, this
is the largest National Institute of Mental Health-funded anorexia
nervosa treatment study. The study will allow for a thorough
evaluation of two types of family therapy and will also test whether
FDA approved antidepressant medication can enhance and prolong the
result. The goal of the study is to improve recovery rates.
"Males and females ages 12 through 18 are the target population, because it is essential to identify and treat the illness in its early stage," says Craig Johnson, Ph.D., director and founder of Laureate Eating Disorders Program. He says that a parent may suspect anorexia nervosa if they have an underweight child that worries about their weight and appears to avoid food obsessively. Dr. Johnson and Ovidio Bermudez, M.D., internationally known eating disorder experts, are the principal investigators at Laureate for this study of two forms of outpatient family therapy. The treatments prescribed in the study, have been tested and shown to be helpful with patients in previous studies at Stanford University School of Medicine and The University of Chicago Hospitals.
After undergoing a screening process, families who qualify will be randomly assigned to one of four treatment combinations. The study is comprised of 16 one-hour family therapy sessions delivered over a nine-month time period and a medication (either fluoxetine or placebo) delivered over 15 months under close medical supervision. The family therapy sessions, medications and medication monitoring are all paid for by the NIMH grant.
This international eating disorders study is being coordinated by Stanford University, and includes six recruitment sites: University of California San Diego, Washington University School of Medicine in Saint Louis, Cornell Medical College, Toronto General Hospital, Sheppard Pratt Health System in Baltimore and Laureate Psychiatric Clinic and Hospital.
Individuals who suspect they might have anorexia nervosa, family members who believe their child may have the illness and physicians of potential patients are urged to call Nancy Morales, RN at 918-491-3722 to learn more about the study and/or apply for participation.
San Diego, CA
: UCSD Researchers Seek Males and Females with
Anorexia Nervosa: The UCSD researchers are currently seeking
adolescents and adults currently suffering from Anorexia Nervosa to
participate in one of their three current studies. To qualify for any of
the studies one must be at least 15% below ideal body weight and be
fearful of weight gain, despite being underweight. Both adults and
adolescents between the ages of 14-45 are needed to participate in a
taste study and would be compensated for up to $70 for completing
the assessments, taste tests and interview. Adults 18 years of age and
older are needed to participate in a randomized control trial of the
medication Quetiapine, in which they will receive either the study
medication or a placebo. Subjects will be compensated up to $360 for
completing study related assessments and the medication treatment.
In addition, they are offering several months of family therapy treatment for families with adolescents between the ages of 12 and 18 at no cost. The adolescents in this study will also be randomly assigned to receive either the medication Fluoxetine or a placebo. For more information, contact UCSD Eating Disorder Treatment and Research Progr
San Diego, CA
: UCSD Researchers Seek Women Recovered From an
Eating Disorder: Help UCSD researchers understand what causes
eating disorders. They are seeking female participants between 18 and
45 years of age who are recovered from Anorexia or Bulimia Nervosa.
By participating in the study, subjects will be assisting physicians and
researchers in developing new treatments for these complex and
serious disorders. Subjects will be compensated for your participation
in this study. For more information contact the UCSD Eating Disorder
Research and Treatment Program at 858-366-2525 or email
Research Study - Massachusetts General Hospital
Study of Therapy for Bone Loss in Anorexia Nervosa: The
Neuroendocrine Unit of Massachusetts General Hospital is conducting
research studies on anorexia-induced bone loss. Their screening study
is for men and women age 12-50 with anorexia nervosa. They are
investigating causes of osteopenia (or bone loss) in the spine, hip,
wrist and total body. The study involves one visit of approximately 3
hours. Their treatment study is for women aged 18-45 with anorexia
nervosa and absent or irregular menstrual periods. They are
investigating the combined use of a natural hormone and a medication
that is effective for bone loss in postmenopausal women as a novel
treatment for the bone loss seen in women with anorexia nervosa.
They hope that the combination of these two investigational
medications will help rebuild depleted bone and prevent further bone
breakdown in women with anorexia nervosa. The study consists of 6 visits over 12 months. A stipend of up to $675 is awarded throughout the course of the study. If interested, call Erinne Meenaghan, N.P. at .
: Bulimia Nervosa Study: Free confidential treatment
is available to those who are eligible. Do you or someone you know
binge eat? Do you or someone you know compensate by vomiting or
other extremes? Do you or someone you know have severe moodiness
or relationship problems? Researchers are now enrolling participants
(ages 18-65) in a free treatment study investigating two active
treatments, including education and counseling, for bulimia nervosa. If
New York, NY
: NIMH-funded, IRB-Approved Study of Adolescents
with Bulimia Nervosa (ages 12 - 21 years). This study takes place at
NYSPI/Columbia University and compensation is provided for
participation ($100). For more information, contact Laura Berner at
212-543-5316. P.I.: Rachel Marsh, Ph.D., Assistant Professor of Clinical
Psychology, Columbia University/ New York State Psychiatric Institute,
phone 212-543-5384, email
New York, NY
: The National Institute of Mental Health is sponsoring a
multi-center international study to compare two types of family
therapy as well as fluoxetine or placebo (an inactive medication) in the
treatment of adolescents with anorexia nervosa. They are looking for
families with an adolescent with anorexia nervosa between the ages of
12-18 years. Participation involves completing assessment interviews,
questionnaires, and engaging in 16 family therapy sessions over the
course of nine months with medication continuing for another six
months. The study is being held at the Eating Disorders Research Program, The Westchester Division of New York-Presbyterian Hospital, Weill Medical College of Cornell University. Contact the Research Coordinator, Samantha Berthod, MA at 914-997-4395.
Seeking Women Recovered from Anorexia or Bulimia
Nervosa. Dr. Walter Kaye and his research team at the Eating
Disorders Research Program at the University Pittsburgh Medical
Center are looking for women who have recovered from anorexia or
bulimia nervosa for a research study on brain chemistry in eating
disorders. Study participants must be between 18 and 45 years old,
medication free (birth control pills acceptable) and not pregnant or
nursing. The study involves phone interviews, questionnaires, PET and
MRI scans, lab work, physical exam, two visits to Pittsburgh and 8
weeks of fluoxetine (generic form of Prozac). (Note: All expenses
incurred during the study, e.g. travel expenses, lab work, physical
exam and etc. are paid for by the study.) In addition, eligible
participants will be compensated up to $1300 upon completion of the
study. For more information, email or Dr.
Kathy Plotnicov at . Sharon Barnes at
1-866-265-9289 or submit a contact form online
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