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Perinatal Diagnosis of GIT Anomalies

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: NCT03514940
Recruitment Status : Recruiting
First Posted : May 3, 2018
Last Update Posted : January 27, 2020
Kasr El Aini Hospital
National Research Center, Egypt
Information provided by (Responsible Party):
Mahmoud Alalfy, Aljazeera Hospital

Brief Summary:
fetal gastro intestinal abnormalities can be accurately diagnosed in second trimester

Condition or disease Intervention/treatment
Fetal Anomalies Diagnostic Test: ultrasound

Detailed Description:
prenatal diagnosis of these anomalies allows for early postnatal interventions and implementation of treatment options

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Study Type : Observational
Estimated Enrollment : 130 participants
Observational Model: Cohort
Time Perspective: Prospective
Official Title: Perinatal Diagnosis of Fetal GIT Anomalies
Actual Study Start Date : May 2, 2018
Estimated Primary Completion Date : June 3, 2020
Estimated Study Completion Date : July 7, 2020

Intervention Details:
  • Diagnostic Test: ultrasound
    second trimester us scan will be made to pregnant women

Primary Outcome Measures :
  1. The number of participants who will be diagnosed to have GIT anomalies [ Time Frame: within 5 moths ]
    GIT anomalies that will be diagnosed by US and confirmed postnatal and managed operatively

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.

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Ages Eligible for Study:   20 Years to 40 Years   (Adult)
Sexes Eligible for Study:   Female
Gender Based Eligibility:   Yes
Gender Eligibility Description:   pregnant females
Accepts Healthy Volunteers:   Yes
Sampling Method:   Probability Sample
Study Population
pregnant ladies either primi or multigravida

Inclusion Criteria:

  • pregnant women either primi or multigravida
  • pregnant in 18- 24 weeks

Exclusion Criteria:

  • first trimester pregnant ladies

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): NCT03514940

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Contact: Mahmoud Alalfy 01002611058

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Algazeerah Recruiting
Giza, Egypt
Contact: Mahmoud Alalfy, master    +201002611058   
Contact: Ahmed Elgazzar, M.D    +201014005959      
Principal Investigator: Mahmoud Alalfy, master         
Sponsors and Collaborators
Aljazeera Hospital
Kasr El Aini Hospital
National Research Center, Egypt
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Principal Investigator: Mahmoud Alalfy, M.s.c Algazeerah hospital -Location (Giza -Egypt ) and National Research centre egypt
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Responsible Party: Mahmoud Alalfy, Assistant Researcher , National Research centre and Specialist of Obstetrics and Gynecology in Aljazeerah hospital, Aljazeera Hospital Identifier: NCT03514940    
Other Study ID Numbers: GIT
First Posted: May 3, 2018    Key Record Dates
Last Update Posted: January 27, 2020
Last Verified: January 2020
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No
Plan Description: results will be published

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Additional relevant MeSH terms:
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Congenital Abnormalities