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POETRY: Study of Estrogen Replacement Therapy in Postmenopausal Women With Parkinson's Disease

Primary Purpose

Parkinson's Disease

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Premarin ®
Sponsored by
The Parkinson Study Group
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Parkinson's Disease focused on measuring Parkinson disease, women, postmenopause, estrogen replacement therapy, clinical trials

Eligibility Criteria

undefined - 75 Years (Child, Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria: Post-menopausal women with Parkinson's disease who experience levodopa-related motor fluctuations averaging at least 2 hours daily in the "off" state confirmed by home diaries Must be on a stable dose of carbidopa/levodopa, immediate or controlled release therapy, antidepressants, or anxiolytics (for the last 30 days) Exclusion Criteria: Insulin dependent diabetes Thyroid disease

Sites / Locations

  • The Parkinson's Institute
  • Emory University
  • Indiana University School of Medicine
  • University of Maryland
  • University of Rochester
  • Duke University Medical Center

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

1

Arm Description

Premarin

Outcomes

Primary Outcome Measures

Safety - Adverse event frequency, vital signs (change from Baseline to Month 2)
Tolerability - Proportion of participants who complete the trial

Secondary Outcome Measures

Motor
Cognition
Behavior
Serum estradiol levels - change from Baseline to Month 2

Full Information

First Posted
October 5, 2005
Last Updated
December 24, 2007
Sponsor
The Parkinson Study Group
Collaborators
Wyeth is now a wholly owned subsidiary of Pfizer, Joseph and Rosalyn Newman Foundation
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1. Study Identification

Unique Protocol Identification Number
NCT00234676
Brief Title
POETRY: Study of Estrogen Replacement Therapy in Postmenopausal Women With Parkinson's Disease
Official Title
A Multi-Center, Double Blind, Randomized, Placebo-Controlled, Parallel Group Study for the Safety, Tolerability and Efficacy of Estrogen Replacement Therapy (Conjugated Equine Estrogens 0.625 mg Daily) in Post Menopausal Women With Parkinson's Disease
Study Type
Interventional

2. Study Status

Record Verification Date
December 2007
Overall Recruitment Status
Completed
Study Start Date
October 2003 (undefined)
Primary Completion Date
March 2006 (Actual)
Study Completion Date
March 2006 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
The Parkinson Study Group
Collaborators
Wyeth is now a wholly owned subsidiary of Pfizer, Joseph and Rosalyn Newman Foundation

4. Oversight

5. Study Description

Brief Summary
The primary objectives of the POETRY study are to assess the safety and tolerability of estrogen replacement therapy (ERT) in postmenopausal women with Parkinson's disease (PD) and to assess recruitment for a study of ERT in postmenopausal women with PD.
Detailed Description
POETRY is an 8-week study of 30 post-menopausal women with Parkinson's disease (PD) who will be enrolled at six clinical sites in the United States. The study is designed to measure the safety and tolerability of estrogen replacement therapy (ERT). The study will also measure how ERT affects thinking and behavior, movement and activities of daily living, as well as motor fluctuations and dyskinesias. Although we know there are gender differences in PD, no studies have assessed their impact on symptom management. Women with PD usually require less levodopa, are more likely to experience drug-related dyskinesia, and commonly report changes of their symptoms with menstruation, menopause and use of hormones, implying that hormonal changes may impact PD symptoms. All perimenopausal women face the decision whether or not to use estrogen replacement therapy (ERT) and for women with PD, information about estrogen's effects in PD may facilitate decision-making.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Parkinson's Disease
Keywords
Parkinson disease, women, postmenopause, estrogen replacement therapy, clinical trials

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
23 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Experimental
Arm Description
Premarin
Intervention Type
Drug
Intervention Name(s)
Premarin ®
Intervention Description
Premarin ® 0.625 mg per day orally
Primary Outcome Measure Information:
Title
Safety - Adverse event frequency, vital signs (change from Baseline to Month 2)
Time Frame
60 days
Title
Tolerability - Proportion of participants who complete the trial
Time Frame
60 days
Secondary Outcome Measure Information:
Title
Motor
Time Frame
60 days
Title
Cognition
Time Frame
60 days
Title
Behavior
Time Frame
60 days
Title
Serum estradiol levels - change from Baseline to Month 2
Time Frame
60 days

10. Eligibility

Sex
Female
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Post-menopausal women with Parkinson's disease who experience levodopa-related motor fluctuations averaging at least 2 hours daily in the "off" state confirmed by home diaries Must be on a stable dose of carbidopa/levodopa, immediate or controlled release therapy, antidepressants, or anxiolytics (for the last 30 days) Exclusion Criteria: Insulin dependent diabetes Thyroid disease
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lisa M Shulman, MD
Organizational Affiliation
University of Maryland
Official's Role
Principal Investigator
Facility Information:
Facility Name
The Parkinson's Institute
City
Sunnyvale
State/Province
California
Country
United States
Facility Name
Emory University
City
Atlanta
State/Province
Georgia
Country
United States
Facility Name
Indiana University School of Medicine
City
Indianapolis
State/Province
Indiana
Country
United States
Facility Name
University of Maryland
City
Baltimore
State/Province
Maryland
Country
United States
Facility Name
University of Rochester
City
Rochester
State/Province
New York
Country
United States
Facility Name
Duke University Medical Center
City
Durham
State/Province
North Carolina
Country
United States

12. IPD Sharing Statement

Links:
URL
http://www.Parkinson-Study-Group.org
Description
Parkinson Study Group

Learn more about this trial

POETRY: Study of Estrogen Replacement Therapy in Postmenopausal Women With Parkinson's Disease

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