Skip to main content
OpenTrials
Completed

NCT Number: NCT00234676

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

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.

Completed

Looking for future studies?

Notify Me

Key information

Age range

Up to 75 year

Sex eligibility

Female

Study type

Interventional

Phase

Phase 2

Primary location

The Parkinson's Institute, Sunnyvale, California, United States

Loading trial locations.

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Premarin ®

Drug

Premarin ® 0.625 mg per day orally

Primary outcomes

  1. Safety - Adverse event frequency, vital signs (change from Baseline to Month 2)

    Time frame: 60 days

  2. Tolerability - Proportion of participants who complete the trial

    Time frame: 60 days

Secondary outcomes

  1. Motor

    Time frame: 60 days

  2. Cognition

    Time frame: 60 days

  3. Behavior

    Time frame: 60 days

  4. Serum estradiol levels - change from Baseline to Month 2

    Time frame: 60 days

Sponsors and collaborators

Lead sponsor

The Parkinson Study Group

Network

Collaborators

  • Joseph and Rosalyn Newman Foundation
  • Wyeth is now a wholly owned subsidiary of Pfizer

Registry information

Official study 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

Important dates

Study start
2003
Primary completion
2006
Study completion
2006
First posted
Oct 7, 2005
Registry last updated
Jan 8, 2008

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.