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Clinical trialNCT00143039TerminatedObservational

Amniotic Fluid Tandem Mass Spectrometry for Pregnancies Complicated by NIH and Severe Symmetrical IUGR

SponsorObstetrix Medical GroupEnrollment48Fetal Growth RetardationHydrops Fetalis
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

The objective of this pilot study is to prospectively evaluate amniotic fluid of pregnancies complicated by non-immune hydrops and severe symmetrical intrauterine growth restriction by tandem mass spectrometry for inborn errors of metabolism.

Investigators

The overall officials registered on this study. Names that resolve to a FindMyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

11 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

United States
  • Banner Desert Samaritan Hospital

    Phoenix, Arizona, United States

  • Banner Good Sammaritan Hospital

    Phoenix, Arizona, United States

  • Saddleback Memorial Medical Center

    Laguna Hills, California, United States

  • Long Beach Memorial Medical Center

    Long Beach, California, United States

  • Good Samaritan Hospital

    San Jose, California, United States

  • Presbyterian/st Luke'S Hospital

    Denver, Colorado, United States

  • Swedish Medical Center

    Denver, Colorado, United States

  • Dekalb Medical Center

    Decatur, Georgia, United States

  • Southern Regional Medical Center

    Riverdale, Georgia, United States

  • Harris Methodist Fort Worth Hospital

    Fort Worth, Texas, United States

  • Swedish Medical Center

    Seattle, Washington, United States

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

No drug or biological interventions are in our data for this study. It may test a procedure, device or behavioral intervention, or the intervention list isn't in our current snapshot. See the registry record ↗. Why? →

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
31 Mar 2006
Primary completion
31 Aug 2009
Completion
31 Aug 2009
Last update posted
19 Dec 2014
Registered enrollment
48
Registry id
NCT00143039

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 24 Aug 2026. Registry facts are shown as registered by the study sponsor; FindMyKOL does not interpret them.