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NCT00361075 · ClinicalTrials.gov registry record · Phase 4

Midlife Cholesterol Study

A Phase 4 study, sponsored by Northwestern University.

Completed
Registry status
Phase 4
Development phase
120
Enrollment target

NCT00361075: Completed Phase 4 study, sponsored by Northwestern University.

NCT00361075 is a Phase 4 study that has completed, run by Northwestern University. The registered enrollment target is 120 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (77% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00361075, a Phase 4 study, has completed, sponsored by Northwestern University.

COMPLETED
Registry status
Phase 4
Development phase
120 participants
Enrollment target

Study Summary

The postmenopausal state is associated with an increase risk for heart disease. Much of this increase in risk may be due to the loss of estrogen (the main female hormone) and the effect of this loss on lipids (blood fats). This loss of estrogen is often treated by estrogen replacement therapy. Estrogen replacement therapy seems to have a beneficial effect on lipid levels. The purpose of this research study is to understand 1) how menopause affects lipids and 2) how hormone replacement therapy effects the lipid metabolism of postmenopausal women.

Interventions

  • DRUG transdermal estradiol patch (Vivelle), oral estrogen (Estrace), progesterone (Prometrium)

Trial Details

FieldValue
Enrollment Target 120 participants
Start Date 1998-07
Est. Completion 2005-05
Phase Phase 4
Northwestern University

1,209 total trials

What the finished NCT00361075 record still lists

NCT00361075 is an interventional study that assigns participants to a tested intervention. The registered 120 participants enrollment target is mid-sized for trials with a published cap, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (77% lower).

The record links to 0 conditions, and to 1 intervention - of which transdermal estradiol patch (Vivelle), oral estrogen (Estrace), progesterone (Prometrium) is the first listed.

NCT00361075 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00361075 about?

NCT00361075 is a clinical study titled "Midlife Cholesterol Study". The postmenopausal state is associated with an increase risk for heart disease. Much of this increase in risk may be due to the loss of estrogen (the main female hormone) and the effect of this loss on lipids (blood fats). This loss of estrogen is often treated by estrogen replacement therapy. Estro...

What is the current status of trial NCT00361075?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 120 participants. The study started on 1998-07. Estimated completion is 2005-05.

What interventions are being tested in trial NCT00361075?

The interventions under investigation include: transdermal estradiol patch (Vivelle), oral estrogen (Estrace), progesterone (Prometrium) (DRUG).

Who is sponsoring clinical trial NCT00361075?

This trial is sponsored by Northwestern University, which has 1,209 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00361075's enrollment target sits among peer trials

120 673rd of 2000 higher than 1,289 of 2,000 other Phase 4 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 4 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00361075, the US trial registry maintained by the National Library of Medicine. NCT00361075 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.