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NCT00260091 · ClinicalTrials.gov registry record · NA

Conventional Infertility Treatment vs. Fast Track to IVF

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

Completed
Registry status
NA
Development phase
503
Enrollment target
7
Study locations

NCT00260091 is a NA study of Infertility that has completed, run by Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD). The registered enrollment target is 503 participants, below the 7,583-participant average among 74 other Infertility trials with a reported enrollment target (93% lower). The trial reports 7 study locations across 1 state.

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The verdict

NCT00260091, a NA study of Infertility, has completed, sponsored by Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD).

COMPLETED
Registry status
NA
Development phase
503 participants
Enrollment target
7
Study locations

Study Summary

The purpose of this randomized prospective clinical trial is to determine whether an infertility treatment that moves quickly to In Vitro Fertilization (IVF) is more cost effective than the usual treatment strategy which includes various combinations of infertility drugs and intrauterine insemination (IUI) prior to utilizing In Vitro Fertilization.

Conditions Studied

Interventions

  • PROCEDURE intrauterine insemination
  • PROCEDURE infertility

Study Locations (7)

Massachusetts

  • Harvard Vanguard Medical Associates - Boston
  • Boston IVf - Brookline
  • Harvard Vanguard Medical Associates - Burlington
  • Boston IVF - Quincy
  • Harvard Vanguard Medical Associates - Quincy
  • Boston IVF - Waltham
  • Harvard Vanguard Medical Associates - Wellesley

Trial Details

FieldValue
Enrollment Target 503 participants
Start Date 1999-08
Est. Completion 2006-04
Phase NA

What the Registry Record Tells You About NCT00260091

The ClinicalTrials.gov registry entry for NCT00260091 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 503 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 7,583-participant average among 74 other Infertility trials with a reported enrollment target (93% lower). The listed sponsor is Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), which has 305 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Infertility appearing as the primary indexed condition, and to 2 interventions - of which intrauterine insemination is the first listed.

NCT00260091 reports 7 study locations spanning 1 distinct geographic area - top geographies include Massachusetts.

Frequently Asked Questions

What is clinical trial NCT00260091 about?

NCT00260091 is a clinical study titled "Conventional Infertility Treatment vs. Fast Track to IVF". The purpose of this randomized prospective clinical trial is to determine whether an infertility treatment that moves quickly to In Vitro Fertilization (IVF) is more cost effective than the usual treatment strategy which includes various combinations of infertility drugs and intrauterine inseminatio...

What is the current status of trial NCT00260091?

This trial is currently completed. It is a NA study. The enrollment target is 503 participants. The study started on 1999-08. Estimated completion is 2006-04.

What conditions does trial NCT00260091 study?

This clinical trial studies the following conditions: Infertility.

What interventions are being tested in trial NCT00260091?

The interventions under investigation include: intrauterine insemination (PROCEDURE), infertility (PROCEDURE).

Who is sponsoring clinical trial NCT00260091?

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.

Where is trial NCT00260091 being conducted?

This trial has 7 study locations across Massachusetts. 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

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.