Trial record 2 of 29 for:    Recruiting, Not yet recruiting, Available Studies | "Hernia, Diaphragmatic"

Proteomic Profiling for Congenital Diaphragmatic Hernia (pro-CDH)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details. Identifier: NCT03179371
Recruitment Status : Recruiting
First Posted : June 7, 2017
Last Update Posted : July 18, 2018
Information provided by (Responsible Party):
Centre Hospitalier Universitaire de Besancon

Brief Summary:

Congenital diaphragmatic hernia (CDH) is a severe congenital malformation, related to a developmental defect of the diaphragm. The incidence of CDH is approximated at 1 in 3,000 live births. Although advances in surgery and neonatal intensive care have improved the prognosis, mortality remains high, around 30-50% related to severe lung hypoplasia and persistent pulmonary hypertension. Prenatal evaluation with observed/expected Lung over Head Ratio (o/e LHR), liver position and total lung volume measured by magnetic resonance, have been shown to correlate with neonatal mortality . However, the preponderant factor of persistent pulmonary hypertension remains difficult to predict prenatally. In patients with isolated diaphragmatic hernia (without associated malformations or karyotype abnormalities), prognosis is evaluated indirectly on pulmonary development from pulmonary volume measurements. Apart from the most caricatural cases with extremely good or very pejorative values, for a large proportion of fetuses with diaphragmatic dome hernia the prognosis remains uncertain.

The aim of the proposal is to investigate whether the analysis of the proteom of the amniotic fluid of the fetuses with CDH could give information of a prognostic character. The objective of the study is to identify, from the proteomic profile of the amniotic fluid of mothers whose fetus has CDH, prognostic markers candidates for death at 2 months of the infant. The first step is to carry out an exploratory and non-interventional study on a small sample (n = 10) of the target population. This is a preliminary step before considering, if the results are encouraging, a large-scale study from a biological collection to determine candidate proteins (new biomarkers) which relative expression levels could be used as surrogate marker of pulmonary hypoplasia.

Condition or disease
Congenital Diaphragmatic Hernia

Detailed Description:

Pregnant patients for whom amniocentesis will be performed as part of the prenatal management of CDH confirmed by fetal ultrasound will be approached fot inclusion in the study. The indication of amniocentesis will be indicated according to the usual standards of care. Briefly, the study will not involve any additional invasive procedure. In our study, amniocentesis will be indicated during the conventional management of these patients. The needs of our research will not lead to additional amniocenteses, but simply an increase in the volume of amniotic fluid collected. An additional volume of 5 ml will be sampled for volumes usually taken from 20 to 30 ml. This volume of sampling will have a very limited impact on maternal and fetal well-being. An analysis of the proteom of the amniotic fluid of the patients will be carried out. The relative amounts of proteins and peptides contained in the amniotic fluid will be analyzed to explore variations in proteomic profile that may reflect different clinical gravity in terms of further evolution. The usual management of the patients and their children will not be modified by the procedures related to the research.

The first step will consist in carrying out a depletion of the major proteins, in particular albumin. A protein assay will be carried out from the same amount of protein for each sample (standardization). This depletion step will be followed by a migration step on a gel of 1D electrophoresis. Its purpose is both to eliminate all the contaminants that can hinder mass spectrometry analysis, to separate the proteins according to their molecular weight in order to simplify the protein mixture and to have a visual control of the heterogeneity of the sample. A differential visual analysis after staining will allow to define the highly variable zones between the groups of patients and within the same sample. We will select the zone of interest in identical manner for each sample and for the whole of the gel track. The use of commercial electrophoresis gels of the same batch and the parallel analysis of several samples of different groups and the use of quality controls ensure reproducibility. The proteins contained in these bands / gel zones are then digested according to a standardized protocol under controlled conditions. The simultaneous treatment of the different biological samples makes it possible to considerably reduce the impact of the variability of this step in the final differential statistical analysis. At the end of this step the proteins are analyzed by an LC-ESI MS / MS approach. This LC-ESI MS / MS approach consists of separating the peptides on a chromatographic separation column which is coupled directly to the ESI-MS / M mass spectrometer. This analytical approach can allow the identification of more than 1000 proteins and 5000 peptides. This analysis is repeated 3 times per sample so that analytical variability can be taken into account in differential statistical studies. At the end of this protocol the raw data of each zone are pooled by sample and the differential statistical study can be carried out.

Study Type : Observational
Estimated Enrollment : 10 participants
Observational Model: Other
Time Perspective: Prospective
Official Title: Proteomic Analysis of Amniotic Fluid in the Case of Diaphragmatic Hernia: Search for Prognostic Expression Profiles
Actual Study Start Date : May 18, 2017
Estimated Primary Completion Date : July 2019
Estimated Study Completion Date : November 2019

Mothers whose fetus has CDH

Primary Outcome Measures :
  1. Neonatal death [ Time Frame: 2 months of age ]

Secondary Outcome Measures :
  1. Prenatal death of the fetus [ Time Frame: 9 months ]
    Death during pregnancy

  2. Neonatal death [ Time Frame: 15 days ]
  3. Apgar score [ Time Frame: 5 min after birth ]
  4. Age at surgery [ Time Frame: 6 months of age ]
  5. Need for a diaphragmatic prosthesis [ Time Frame: 6 months of age ]
  6. Duration of ventilation (in days) [ Time Frame: 6 months of age ]
  7. Duration of the oxygen dependency (in days) [ Time Frame: 6 months of age ]
  8. Need of supplemental oxygen therapy [ Time Frame: 28 days of age ]
    Binary outcome (Yes/No)

  9. Occurrence of pulmonary hypertension [ Time Frame: 6 months of age ]
  10. Duration of parenteral nutrition (in days) [ Time Frame: 6 months of age ]
  11. Age at the beginning of enteral nutrition [ Time Frame: 6 months of age ]
  12. Age at the beginning of oral nutrition [ Time Frame: 6 months of age ]
  13. Duration of hospital stay (in days) [ Time Frame: 6 months of age ]

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 50 Years   (Adult)
Sexes Eligible for Study:   Female
Gender Based Eligibility:   Yes
Gender Eligibility Description:   Pregnant females
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population
Mothers whose fetus has CDH

Inclusion Criteria:

Pregnant patients for whom amniocentesis will be performed as part of the prenatal diagnosis of a diaphragmatic hernia.

Exclusion Criteria:

  • Refusal of patients,
  • Refusal of spouse regarding data of the future child,
  • Multiple malformations,
  • Twin pregnancy,
  • Prenatal diagnosis of an unconfirmed diaphragmatic hernia,
  • Miscarriage after amniocentesis.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT03179371

Contact: Frédéric Auber, Professor + 33 3 81 21 82 21

CHU de Besançon Active, not recruiting
Besançon, France, 25000
CHU de Dijon Recruiting
Dijon, France, 21000
Contact: Thierry ROUSSEAU, MD, PhD   
Sponsors and Collaborators
Centre Hospitalier Universitaire de Besancon

Responsible Party: Centre Hospitalier Universitaire de Besancon Identifier: NCT03179371     History of Changes
Other Study ID Numbers: API/2016/78
First Posted: June 7, 2017    Key Record Dates
Last Update Posted: July 18, 2018
Last Verified: July 2018
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No

Additional relevant MeSH terms:
Hernia, Diaphragmatic
Hernias, Diaphragmatic, Congenital
Pathological Conditions, Anatomical
Congenital Abnormalities