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CompletedNCT01184469Updated Oct 15, 2012

Prospective Observational Study of Peri-implantation Serum hCG Levels

An observational study in Infertility, sponsored by Bruce Shapiro M.D.. Completed at 1 site in United States. Open to female participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2012-10-15.

Sponsored by Bruce Shapiro M.D. · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
451
Ages
18 Years and older
Sex
Female
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Study summary

The purpose of this study is to prospectively define a set of data suitable for developing models of pregnancy viability. Those models will be based on serum hCG concentration measured during the peri-implantation period in patients that received fresh embryo transfer and those that received transfer of frozen-thawed embryos, and to compare and contrast these models. This may reveal insights into differences between these types of IVF cycles.

Read the detailed description

The current study seeks to examine the effect of the timing of implantation (as indicated by the first increase in serum hCG level) on the viability of pregnancies and to determine if such effect of timing differs between fresh embryo transfers and frozen-thawed embryos transfers. In this case, the timing of implantation will be measured through serum hCG analysis on days 3, 4, 5, and 7 after blastocyst transfer.

02

Conditions studied

  • Infertility

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03

In context

Infertility

2,506 studies on the registry are indexed under Infertility; 407 are open to participants now.

This study's enrollment of 451 is above the median of 200 across 714 observational studies indexed under Infertility.

Browse Infertility studies →

Lead sponsor

Bruce Shapiro M.D. is the lead sponsor of 4 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
Female
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

IVF patients

Inclusion criteria

  • IVF patients (adults) who received blastocyst transfer

Exclusion criteria

Exclusion Criteria:

  • Those patients using different laboratories
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
451 participants (actual)

Groups and cohorts

  • Fresh embryo transfers

    Patients who received fresh blastocyst transfer

  • Thawed embryo transfers

    Patients who received transfers of frozen/thawed embryos

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What researchers measure

Primary outcomes

  1. Ongoing pregnancy

    Fetal heart motion at 10 weeks gestation.

    Time frame: 10 weeks gestation

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Study locations

1 site
  • Fertility Center of Las Vegas
    Las Vegas, Nevada 89117, United States
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 15, 2012, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT01184469
Lead sponsor
Bruce Shapiro M.D.
Responsible party
Bruce Shapiro M.D. (Medica Director, Fertility Center of Las Vegas) — Sponsor-investigator
First posted
Aug 19, 2010
Start date
Aug 2010
Primary completion
Mar 2012
Completion
May 2012
Last update
Oct 15, 2012

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Oct 2012. You cannot join it, but the record below documents what was studied.

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