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NCT00532246 · ClinicalTrials.gov registry record · Phase 4

Carotid Artery Intima-Media Thickness Following Exposure to Raloxifene or Placebo

A Phase 4 study of Osteoporosis, Postmenopausal, sponsored by Eli Lilly and Company.

Completed
Registry status
Phase 4
Development phase
147
Enrollment target
5
Study locations

NCT00532246: Completed Phase 4 study of Osteoporosis, Postmenopausal, sponsored by Eli Lilly and Company.

NCT00532246 is a Phase 4 study of Osteoporosis, Postmenopausal that has completed, run by Eli Lilly and Company. The registered enrollment target is 147 participants, below the 2,722-participant average among 12 other Osteoporosis, Postmenopausal trials with a reported enrollment target (95% lower). The trial reports 5 study locations across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00532246, a Phase 4 study of Osteoporosis, Postmenopausal, has completed, sponsored by Eli Lilly and Company.

COMPLETED
Registry status
Phase 4
Development phase
147 participants
Enrollment target
5
Study locations

Study Summary

The purpose of this study is to measure carotid artery IMT at a single visit in a subset of women previously enrolled in the CORE (H3S-MC-GGJY) trial

Interventions

  • DRUG Placebo
  • DRUG raloxifene

Study Locations (5)

California

  • For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician. - La Jolla
  • For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician. - Menlo Park
  • For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician. - Oakland
  • For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician. - San Diego
  • For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician. - Walnut Creek

Trial Details

FieldValue
Enrollment Target 147 participants
Start Date 2003-03
Est. Completion 2003-08
Phase Phase 4
Eli Lilly and Company

1,341 total trials

What the finished NCT00532246 record still lists

NCT00532246 is an interventional study that assigns participants to a tested intervention. The registered 147 participants enrollment target is mid-sized for trials with a published cap, below the 2,722-participant average among 12 other Osteoporosis, Postmenopausal trials with a reported enrollment target (95% lower).

The record links to 1 condition, with Osteoporosis, Postmenopausal appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.

NCT00532246 lists 5 locations in 1 state (California).

Frequently Asked Questions

What is clinical trial NCT00532246 about?

NCT00532246 is a clinical study titled "Carotid Artery Intima-Media Thickness Following Exposure to Raloxifene or Placebo". The purpose of this study is to measure carotid artery IMT at a single visit in a subset of women previously enrolled in the CORE (H3S-MC-GGJY) trial

What is the current status of trial NCT00532246?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 147 participants. The study started on 2003-03. Estimated completion is 2003-08.

What conditions does trial NCT00532246 study?

This clinical trial studies the following conditions: Osteoporosis, Postmenopausal.

What interventions are being tested in trial NCT00532246?

The interventions under investigation include: Placebo (DRUG), raloxifene (DRUG).

Who is sponsoring clinical trial NCT00532246?

This trial is sponsored by Eli Lilly and Company, which has 1,341 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00532246 being conducted?

This trial has 5 study locations across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Osteoporosis, Postmenopausal

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT00532246's enrollment target sits among peer trials

147 5th of 12 higher than 8 of 12 other Osteoporosis, Postmenopausal trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Osteoporosis, Postmenopausal 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 NCT00532246, the US trial registry maintained by the National Library of Medicine. NCT00532246 (mid enrollment · multi site footprint · completed) retrieved and formatted by PlainTrial, see methodology.