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NCT00475553 · ClinicalTrials.gov registry record · NA

Management of Breakthrough Bleeding During Extended Therapy Use With NuvaRing®

A NA study of Breakthrough Bleeding and Breakthrough Spotting, sponsored by Scott and White Hospital & Clinic.

Completed
Registry status
NA
Development phase
75
Enrollment target
1
Study location

NCT00475553 is a NA study of Breakthrough Bleeding and Breakthrough Spotting that has completed, run by Scott and White Hospital & Clinic. The registered enrollment target is 75 participants. The trial reports 1 study location across 1 state.

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The verdict

NCT00475553, a NA study of Breakthrough Bleeding and Breakthrough Spotting, has completed, sponsored by Scott and White Hospital & Clinic.

COMPLETED
Registry status
NA
Development phase
75 participants
Enrollment target
1
Study location

Study Summary

The purpose of this research study is to evaluate the best way to manage breakthrough spotting and bleeding during an extended use regimen of NuvaRing®. Ease of use and acceptability of a flexible regimen of NuvaRing® will also be evaluated. A comparison of cyclic mood symptoms, pelvic pain, and headaches will be made between a standard 21/7 regimen and an extended regimen.

Interventions

  • OTHER remove ring if bleeding or spotting occurs more than 5 days
  • OTHER If bleeding does not remove ring

Study Locations (1)

Texas

  • Scott & White Hospital and Clinic - Temple

Trial Details

FieldValue
Enrollment Target 75 participants
Start Date 2006-05
Est. Completion 2008-05
Phase NA

What the Registry Record Tells You About NCT00475553

The ClinicalTrials.gov registry entry for NCT00475553 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 75 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Scott and White Hospital & Clinic, which has 9 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Breakthrough Bleeding appearing as the primary indexed condition, and to 2 interventions - of which remove ring if bleeding or spotting occurs more than 5 days is the first listed.

NCT00475553 reports 1 study location spanning 1 distinct geographic area - top geographies include Texas.

Frequently Asked Questions

What is clinical trial NCT00475553 about?

NCT00475553 is a clinical study titled "Management of Breakthrough Bleeding During Extended Therapy Use With NuvaRing®". The purpose of this research study is to evaluate the best way to manage breakthrough spotting and bleeding during an extended use regimen of NuvaRing®. Ease of use and acceptability of a flexible regimen of NuvaRing® will also be evaluated. A comparison of cyclic mood symptoms, pelvic pain, and hea...

What is the current status of trial NCT00475553?

This trial is currently completed. It is a NA study. The enrollment target is 75 participants. The study started on 2006-05. Estimated completion is 2008-05.

What conditions does trial NCT00475553 study?

This clinical trial studies the following conditions: Breakthrough Bleeding, Breakthrough Spotting.

What interventions are being tested in trial NCT00475553?

The interventions under investigation include: remove ring if bleeding or spotting occurs more than 5 days (OTHER), If bleeding does not remove ring (OTHER).

Who is sponsoring clinical trial NCT00475553?

This trial is sponsored by Scott and White Hospital & Clinic, which has 9 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00475553 being conducted?

This trial has 1 study location across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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