Study of PET Scans and Serotonin in Hot Flashes Treatment
Primary Purpose
Hot Flashes
Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Paroxetine controlled-release
Conjugated equine estrogen
Sponsored by
About this trial
This is an interventional treatment trial for Hot Flashes focused on measuring Hot flashes, vasomotor symptoms, estrogen, paroxetine
Eligibility Criteria
Inclusion Criteria: Postmenopausal women 7 or more hot flashes per day for at least 3 months Must be able to undergo magnetic resonance (MR) and PET imaging Must be able to receive either paroxetine or estrogen Exclusion Criteria: No treatment with hormone therapy or other medications that affect estrogen within the past 3 months No evidence of a currently active cancer
Sites / Locations
- Johns Hopkins University School of Medicine
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Experimental
Arm Label
Paroxetine
Conjugated equine estrogen
Arm Description
Paroxetine controlled-release (2-12.5 mg tablets, orally, every day for 4 weeks)
Conjugated equine estrogen (0.625 mg tablet, orally, every day for 4 weeks)
Outcomes
Primary Outcome Measures
To estimate the proportion of women who have a 50% or greater reduction in frequency of hot flashes following 4 weeks of paroxetine or conjugated equine estrogen.
To evaluate baseline and change in binding of the serotonin transporter in postmenopausal women who suffer hot flashes before and after 4 weeks of paroxetine or conjugated equine estrogen using PET.
To correlate baseline and change in binding of the serotonin transporter using PET with reduction of hot flashes after 4 weeks of conjugated equine estrogen or paroxetine.
Secondary Outcome Measures
Full Information
NCT ID
NCT00249847
First Posted
November 4, 2005
Last Updated
October 1, 2014
Sponsor
Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins
1. Study Identification
Unique Protocol Identification Number
NCT00249847
Brief Title
Study of PET Scans and Serotonin in Hot Flashes Treatment
Official Title
A Feasibility Study of Positron Emission Tomography (PET) of the Serotonin Transporter (SERT) Before and After Treatment With Conjugated Equine Estrogen or Paroxetine for Hot Flashes
Study Type
Interventional
2. Study Status
Record Verification Date
October 2014
Overall Recruitment Status
Terminated
Why Stopped
Unable to complete accrual; elected to close the study in April 2008.
Study Start Date
October 2005 (undefined)
Primary Completion Date
July 2007 (Actual)
Study Completion Date
April 2008 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The purpose of this study is to determine in a preliminary manner whether successful therapy of hot flashes can be associated with changes in the serotonin transporter in the brain. The serotonin transporter is important in delivering serotonin into certain portions of the brains (serotonin is a chemical that is important in the control of body temperature, mood, sleep, and other functions).
Detailed Description
Hot flashes represent the most common complaint among peri- and postmenopausal women. Over 60% of postmenopausal women experience hot flashes, and 10-20% of all postmenopausal women find them nearly intolerable. Despite the prevalence of hot flashes, their pathophysiology is not well understood. Treatment options include non-pharmacological approaches, hormonal interventions, and non-hormonal pharmacological agents. The most effective treatment for hot flashes is estrogen. The most promising non-hormonal treatments for hot flashes are selective serotonin or noradrenergic reuptake inhibitors (SSRI/SNRI). Although estrogen withdrawal is implicated in the initiation of hot flashes, and serotonin's role is well established in thermoregulation, the relationship between estrogen and serotonin is not known. Preclinical studies suggest that both estrogen and SSRI down regulate the serotonin transporter. Clinical studies that further delineate the relationship between effective treatments for hot flashes and the serotonin transporter may shed a new light into the pathophysiology of these symptoms and more importantly, into design of new-targeted treatments.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hot Flashes
Keywords
Hot flashes, vasomotor symptoms, estrogen, paroxetine
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
5 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Paroxetine
Arm Type
Experimental
Arm Description
Paroxetine controlled-release (2-12.5 mg tablets, orally, every day for 4 weeks)
Arm Title
Conjugated equine estrogen
Arm Type
Experimental
Arm Description
Conjugated equine estrogen (0.625 mg tablet, orally, every day for 4 weeks)
Intervention Type
Drug
Intervention Name(s)
Paroxetine controlled-release
Other Intervention Name(s)
Paxil CR
Intervention Description
2-12.5 mg tablets, orally, every day for 4 weeks
Intervention Type
Drug
Intervention Name(s)
Conjugated equine estrogen
Other Intervention Name(s)
Premarin
Intervention Description
0.625 mg tablet, orally, every day for 4 weeks
Primary Outcome Measure Information:
Title
To estimate the proportion of women who have a 50% or greater reduction in frequency of hot flashes following 4 weeks of paroxetine or conjugated equine estrogen.
Time Frame
Following 4 weeks of study medication
Title
To evaluate baseline and change in binding of the serotonin transporter in postmenopausal women who suffer hot flashes before and after 4 weeks of paroxetine or conjugated equine estrogen using PET.
Time Frame
Following 4 weeks of study medication
Title
To correlate baseline and change in binding of the serotonin transporter using PET with reduction of hot flashes after 4 weeks of conjugated equine estrogen or paroxetine.
Time Frame
Following 4 weeks of study medication
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Postmenopausal women
7 or more hot flashes per day for at least 3 months
Must be able to undergo magnetic resonance (MR) and PET imaging
Must be able to receive either paroxetine or estrogen
Exclusion Criteria:
No treatment with hormone therapy or other medications that affect estrogen within the past 3 months
No evidence of a currently active cancer
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Vered Stearns, MD
Organizational Affiliation
Johns Hopkins University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Johns Hopkins University School of Medicine
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21231
Country
United States
12. IPD Sharing Statement
Learn more about this trial
Study of PET Scans and Serotonin in Hot Flashes Treatment
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