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NCT00950118 · ClinicalTrials.gov registry record

Diaphragmatic Hernia Research & Exploration, Advancing Molecular Science

A clinical trial of Congenital Diaphragmatic Hernia, sponsored by Columbia University.

Recruiting
Registry status
3,000
Enrollment target
14
Study locations

NCT00950118: Recruiting study of Congenital Diaphragmatic Hernia, sponsored by Columbia University.

NCT00950118 is a study of Congenital Diaphragmatic Hernia that is actively recruiting participants, run by Columbia University. The registered enrollment target is 3,000 participants, above the 60-participant average among 22 other Congenital Diaphragmatic Hernia trials with a reported enrollment target (4900% higher). The trial reports 14 study locations across 12 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00950118, a study of Congenital Diaphragmatic Hernia, is actively recruiting participants, sponsored by Columbia University.

RECRUITING
Registry status
3,000 participants
Enrollment target
14
Study locations

Study Summary

The goal of this study is to identify genes that convey susceptibility to congenital diaphragmatic hernia in humans. The identification of such genes, and examination of their structure and function, will enable a delineation of molecular pathogenesis and, ultimately, prevention or treatment of congenital diaphragmatic hernia. There are many different possible modes of inheritance for congenital anomalies, including autosomal dominant, autosomal recessive, and multifactorial. Multi-factorial inheritance is responsible for many common medical disorders, including hypertension, myocardial infarction, diabetes and cancer. This type of inheritance pattern appears to involve environmental factors as well as a combination of genetic variations that together can predispose to or produce congenital anomalies, such as congenital diaphragmatic hernia. Our study is designed to establish a small, well-defined genetic resource consisting of 1) Nuclear families suitable for linkage analysis by parametric,non-parametric (e.g. sib pairs, TDT) and association techniques, 2) Individuals with congenital diaphragmatic hernia who can be directly screened for allelic variation in candidate genes, and 3) Individuals who can serve as controls (are unaffected by congenital diaphragmatic hernia). Neonates and their families will be collected from homogenous and heterogeneous populations. By characterizing diverse populations, it should be possible to increase the likelihood of demonstration of genetic variation in selected candidate genes that can then be used in association and linkage studies in individual subjects with congenital diaphragmatic hernia.

Primary Outcome

DNA samples from patients will be analyzed for underlying genetic causes.

Study Locations (14)

New York

  • Northwell Health - Manhasset
  • New York University, Hassenfeld Children's Hospital at NYU Langone Health - New York
  • Morgan Stanley Children's Hospital of New York- Presbyterian (Columbia University Medical Center) - New York

Illinois

  • Rush Hospital - Chicago

Michigan

  • University of Michigan/ CS Mott Children's Hospital - Ann Arbor

Missouri

  • Washington University Medical Center/ St. Louis Children's Hospital - St Louis

Nebraska

  • Children's Hospital of Omaha/ University of Nebraska - Omaha

Ohio

  • Cincinnati Children's Hospital and Medical Center/ University of Cincinnati - Cincinnati

Oregon

  • Oregon Health & Science University, Doernbecher Children's Hospital - Portland

Pennsylvania

  • Children's Hospital of Pittsburgh/ University of Pittsburgh - Pittsburgh

Trial Details

FieldValue
Enrollment Target 3,000 participants
Start Date 2005-06
Est. Completion 2026-09
Columbia University

958 total trials

What NCT00950118 shows while recruiting

NCT00950118 is an observational study that tracks outcomes without assigning an intervention. Its 3,000 participants enrollment target places it among the larger protocols in the corpus, above the 60-participant average among 22 other Congenital Diaphragmatic Hernia trials with a reported enrollment target (4900% higher).

The record links to 1 condition, with Congenital Diaphragmatic Hernia appearing as the primary indexed condition, and to 0 interventions.

NCT00950118 lists 14 locations in 12 states (New York, Illinois, Michigan).

Frequently Asked Questions

What is clinical trial NCT00950118 about?

NCT00950118 is a clinical study titled "Diaphragmatic Hernia Research & Exploration, Advancing Molecular Science". The goal of this study is to identify genes that convey susceptibility to congenital diaphragmatic hernia in humans. The identification of such genes, and examination of their structure and function, will enable a delineation of molecular pathogenesis and, ultimately, prevention or treatment of cong...

What is the current status of trial NCT00950118?

This trial is currently recruiting. The enrollment target is 3,000 participants. The study started on 2005-06. Estimated completion is 2026-09.

What conditions does trial NCT00950118 study?

This clinical trial studies the following conditions: Congenital Diaphragmatic Hernia.

Who is sponsoring clinical trial NCT00950118?

This trial is sponsored by Columbia University, which has 958 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00950118 being conducted?

This trial has 14 study locations across Illinois, Michigan, Missouri, Nebraska, New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Congenital Diaphragmatic Hernia

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT00950118's enrollment target sits among peer trials

3,000 1st of 22 higher than 22 of 22 other Congenital Diaphragmatic Hernia trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Congenital Diaphragmatic Hernia trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00950118, the US trial registry maintained by the National Library of Medicine. NCT00950118 (large enrollment · multi site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.