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NCT02254577 · ClinicalTrials.gov registry record · Phase 4

Vaginal Compared to Intramuscular Progesterone for Frozen Embryo Transfer

A Phase 4 study of Infertility, sponsored by Shady Grove Fertility Reproductive Science Center.

Completed
Registry status
Phase 4
Development phase
1,139
Enrollment target
14
Study locations

NCT02254577 is a Phase 4 study of Infertility that has completed, run by Shady Grove Fertility Reproductive Science Center. The registered enrollment target is 1,139 participants, below the 7,574-participant average among 74 other Infertility trials with a reported enrollment target (85% lower). The trial reports 14 study locations across 4 states.

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The verdict

NCT02254577, a Phase 4 study of Infertility, has completed, sponsored by Shady Grove Fertility Reproductive Science Center.

COMPLETED
Registry status
Phase 4
Development phase
1,139 participants
Enrollment target
14
Study locations

Study Summary

To determine whether the of vaginal progesterone replacement for frozen embryo transfer results in equivalent live birth rates to intramuscular injection progesterone replacement.

Conditions Studied

Interventions

  • DRUG Endometrin® plus Progesterone in Oil (PIO)
  • DRUG Progesterone in Oil (PIO) Only

Study Locations (14)

Maryland

  • Shady Grove Fertility Center - Annapolis
  • Shady Grove Fertility Center - Baltimore
  • Shady Grove Fertility Center - Bel Air
  • Shady Grove Fertility Center - Columbia
  • Shady Grove Fertility Center - Frederick
  • Shady Grove Fertility Center - Rockville
  • Shady Grove Fertility Center - Towson

Virginia

  • Shady Grove Fertility Center - Annandale
  • Shady Grove Fertility Center - Leesburg
  • Shady Grove Fertility Center - Woodbridge

District of Columbia

  • Shady Grove Fertility Center - Washington D.C.
  • Shady Grove Fertility Center - Washington D.C.

Pennsylvania

  • Shady Grove Fertility - Camp Hill
  • Shady Grove Fertility Center - Chesterbrook

Trial Details

FieldValue
Enrollment Target 1,139 participants
Start Date 2014-10
Est. Completion 2018-04-27
Phase Phase 4

What the Registry Record Tells You About NCT02254577

The ClinicalTrials.gov registry entry for NCT02254577 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 1,139 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 7,574-participant average among 74 other Infertility trials with a reported enrollment target (85% lower). The listed sponsor is Shady Grove Fertility Reproductive Science Center, which has 6 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 Endometrin® plus Progesterone in Oil (PIO) is the first listed.

NCT02254577 reports 14 study locations spanning 4 distinct geographic areas - top geographies include Maryland, Virginia, District of Columbia.

Frequently Asked Questions

What is clinical trial NCT02254577 about?

NCT02254577 is a clinical study titled "Vaginal Compared to Intramuscular Progesterone for Frozen Embryo Transfer". To determine whether the of vaginal progesterone replacement for frozen embryo transfer results in equivalent live birth rates to intramuscular injection progesterone replacement.

What is the current status of trial NCT02254577?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 1,139 participants. The study started on 2014-10. Estimated completion is 2018-04-27.

What conditions does trial NCT02254577 study?

This clinical trial studies the following conditions: Infertility.

What interventions are being tested in trial NCT02254577?

The interventions under investigation include: Endometrin® plus Progesterone in Oil (PIO) (DRUG), Progesterone in Oil (PIO) Only (DRUG).

Who is sponsoring clinical trial NCT02254577?

This trial is sponsored by Shady Grove Fertility Reproductive Science Center, which has 6 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02254577 being conducted?

This trial has 14 study locations across District of Columbia, Maryland, Pennsylvania, Virginia. 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.