Serotonin Transporter Concentrations in Women With a History of Anorexia Nervosa
A Positron Emission Tomography Study of the Serotonin Transporter in Weight-Restored Women With Anorexia Nervosa
3 other identifiers
observational
20
1 country
1
Brief Summary
This study will compare the concentrations of serotonin transporter in the brains of women with a history of anorexia nervosa who are currently maintaining a normal weight to those of healthy women of normal weight.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for all trials
Started Jul 2003
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
July 1, 2003
CompletedFirst Submitted
Initial submission to the registry
May 1, 2006
CompletedFirst Posted
Study publicly available on registry
May 3, 2006
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 1, 2009
CompletedStudy Completion
Last participant's last visit for all outcomes
June 1, 2009
CompletedJuly 2, 2012
June 1, 2012
5.9 years
May 1, 2006
June 28, 2012
Conditions
Keywords
Study Arms (2)
1
Women who have had anorexia nervosa but are now maintaining a healthy weight
2
Women who have never had anorexia nervosa and are maintaining a healthy weight
Eligibility Criteria
Participants will be women who have recovered from anorexia nervosa and are currently living in the local community.
You may qualify if:
- History of anorexia nervosa
- BMI has been greater than 18.5 kg/m² for at least 9 months
- Agrees to use an effective method of contraception
- Off all psychotropic and other types of medications likely to impact the serotonin system for at least 21 days
You may not qualify if:
- Use of any psychotropic medication or other types of medications that are likely to affect the serotonin system within 21 days of study entry
- Current DSM-IV Axis-I diagnosis of any illness other than an eating disorder
- Current AN or history of AN within 9 months prior to study entry
- Presence of any psychiatric symptom that would make participation unsafe
- Significant active physical illnesses, particularly those that may affect the brain or serotonergic system, including the following: blood dyscrasias lymphomas; hypersplenism; endocrinopathies; renal failure or chronic obstructive lung disease; autonomic neuropathies; low hemoglobin; anemia; peripheral vascular disease; and malignancy
- Currently receiving effective medication treatment for an eating disorder
- History of Raynaud's phenomena and/or acrocyanosis
- Significant regular tobacco use (defined as more than 1 pack per week)
- Lacks capacity to consent
- Pregnant
- Breastfeeding
- Any metal implants, pacemaker, metal prostheses, orthodontic appliances, or the presence of shrapnel
- Significant history of claustrophobia that would complicate the completion of MRI
- Current or past radiation exposure in the workplace or as part of a research protocol in the previous year
- Badged for radiation
- +11 more criteria
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
New York State Psychiatric Institute
New York, New York, 10032, United States
Related Links
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Evelyn Attia, MD
New York State Psyciatric Institute
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
May 1, 2006
First Posted
May 3, 2006
Study Start
July 1, 2003
Primary Completion
June 1, 2009
Study Completion
June 1, 2009
Last Updated
July 2, 2012
Record last verified: 2012-06