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Heart Rate Variability in Children Conceived Via Assisted Reproductive Technologies

NCT ID: NCT00993369

Last Updated: 2016-11-10

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

60 participants

Study Classification

OBSERVATIONAL

Study Start Date

2006-07-31

Study Completion Date

2010-07-31

Brief Summary

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This is a proof of principle study that investigates heart rate variability differences in fetal and neonatal life in a longitudinal study design and compares two subject groups, offspring conceived using in-vitro fertilization and conceived naturally.

Detailed Description

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This is a proof of principle study that investigates heart rate variability differences in fetal and neonatal life in a longitudinal study design and compares two subject groups, offspring conceived using in-vitro fertilization and conceived naturally.

Conditions

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Neuro Developmental Delay

Keywords

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Prediction of neuro developmental delay

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

PROSPECTIVE

Study Groups

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Healthy newborns conceived naturally

Holter monitor

Intervention Type OTHER

Record heart rate for 2 to 6 hours on day of life 1 or 2.

Healthy newborns conceived with IVF

Holter monitor

Intervention Type OTHER

Record heart rate for 2 to 6 hours on day of life 1 or 2.

Interventions

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Holter monitor

Record heart rate for 2 to 6 hours on day of life 1 or 2.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Fetus or newborn
* Delivery at University of Utah Medical Center, Latter Day Saints Hospital or Intermountain Medical Center

Exclusion Criteria

* Twins
* Genetic anomaly
* Congenital malformation
* Need for special care
Maximum Eligible Age

1 Day

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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University of Utah

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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University of Utah Medical Center

Salt LakeCity, Utah, United States

Site Status

Countries

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United States

Other Identifiers

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00018811

Identifier Type: -

Identifier Source: org_study_id