Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00067509 · ClinicalTrials.gov registry record · Phase 4

Emergency Contraception (ECP): Reducing Unintended Pregnancies

A Phase 4 study, sponsored by Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD).

Completed
Registry status
Phase 4
Development phase
1,100
Enrollment target

NCT00067509: Completed Phase 4 study, sponsored by Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD).

NCT00067509 is a Phase 4 study that has completed, run by Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD). The registered enrollment target is 1,100 participants, above the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (112% higher). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00067509, a Phase 4 study, has completed, sponsored by Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD).

COMPLETED
Registry status
Phase 4
Development phase
1,100 participants
Enrollment target

Study Summary

Emergency contraception is a method of birth control that can be used up to three days after sexual intercourse. Emergency contraceptive pills (ECPs) can be given to a woman before she needs them (advance provision) or when she needs them (emergency provision). This study will compare these two methods of providing ECPs.

Interventions

  • DRUG emergency contraception (estrogen/progesterone)

Trial Details

FieldValue
Enrollment Target 1,100 participants
Start Date 2001-06
Est. Completion 2004-05
Phase Phase 4

What the finished NCT00067509 record still lists

NCT00067509 is an interventional study that assigns participants to a tested intervention. Its 1,100 participants enrollment target places it among the larger protocols in the corpus, above the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (112% higher).

The record links to 0 conditions, and to 1 intervention - of which emergency contraception (estrogen/progesterone) is the first listed.

NCT00067509 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00067509 about?

NCT00067509 is a clinical study titled "Emergency Contraception (ECP): Reducing Unintended Pregnancies". Emergency contraception is a method of birth control that can be used up to three days after sexual intercourse. Emergency contraceptive pills (ECPs) can be given to a woman before she needs them (advance provision) or when she needs them (emergency provision). This study will compare these two meth...

What is the current status of trial NCT00067509?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 1,100 participants. The study started on 2001-06. Estimated completion is 2004-05.

What interventions are being tested in trial NCT00067509?

The interventions under investigation include: emergency contraception (estrogen/progesterone) (DRUG).

Who is sponsoring clinical trial NCT00067509?

This trial is sponsored by Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), which has 305 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00067509's enrollment target sits among peer trials

1,100 65th of 2000 higher than 1,936 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT00710112 · 1,100 participants

    Genetic Variants and Susceptibility to Diseases of Prematurity in Very Low Birth-Weight Infants

  • NCT02688517 · 1,100 participants

    Targeted Genomic Analysis of Blood and Tissue Samples From Patients With Cancer

  • NCT04743765 · 1,100 participants · NA

    HIP Fracture Accelerated Surgical TreaTment And Care tracK 2 Trial

  • NCT05638581 · 1,100 participants · Phase 3

    Trauma Resuscitation With Low-Titer Group O Whole Blood or Products

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT00067509, the US trial registry maintained by the National Library of Medicine. NCT00067509 (large enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.