We updated the design of this site on September 25th. Learn more.
Show more
ClinicalTrials.gov
ClinicalTrials.gov Menu
Trial record 3 of 96 for:    Recruiting, Active, not recruiting Studies | breastfeeding

Breast Feeding Practice in High Risk Pregnant Women

This study is currently recruiting participants.
Verified July 2017 by Ahmed Mohamed Abbas, Assiut University
Sponsor:
ClinicalTrials.gov Identifier:
NCT03178916
First Posted: June 7, 2017
Last Update Posted: July 13, 2017
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.
Information provided by (Responsible Party):
Ahmed Mohamed Abbas, Assiut University
  Purpose
The American Academy of Paediatrics recognizes multiple benefits of breastfeeding to both the term and premature newborn, particularly with regard to protection from infectious agents. Studies have demonstrated decreased rates of bacteraemia, meningitis, respiratory and urinary tract infections, necrotizing enterocolitis, and otitis media among breastfed infants

Condition
Breast Feeding

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective
Official Title: Breast Feeding Practice in High Risk Pregnant Women

Resource links provided by NLM:


Further study details as provided by Ahmed Mohamed Abbas, Assiut University:

Primary Outcome Measures:
  • The number of breast feeding women during pregnancy [ Time Frame: 6 months ]

Estimated Enrollment: 140
Actual Study Start Date: July 1, 2017
Estimated Study Completion Date: October 2018
Estimated Primary Completion Date: June 2018 (Final data collection date for primary outcome measure)
Groups/Cohorts
Low risk pregnant women
evaluation of the efficacy of breastfeeding Low risk pregnant women
high risk pregnant women
evaluation of the efficacy of breastfeeding high risk pregnant women

  Eligibility

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.


Ages Eligible for Study:   20 Years to 45 Years   (Adult)
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population
Patients attending Sohag general hospital
Criteria

Inclusion Criteria:

  1. Diabetes mellitus.
  2. Cardiac disease.
  3. Essential hypertension.
  4. Chronic chest disease, and/or chronic TB infection.
  5. Chronic hepatitis.
  6. Neurologic disease.
  7. Anaemia (Hemoglobin <10 gm/dL).
  8. Thyroid disease.
  9. Multiple pregnancy.

Exclusion Criteria:

  • pregnant women < 34 weeks.
  Contacts and Locations
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 ClinicalTrials.gov identifier (NCT number): NCT03178916


Contacts
Contact: Eman Sedky, MSc 00201010379880 dremanog3@gmail.com

Locations
Egypt
Assiut Faculty of Medicine Recruiting
Assiut, Egypt
Contact: Ahmed Abbas, MD       bmr90@hotmail.com   
Sponsors and Collaborators
Assiut University
  More Information

Responsible Party: Ahmed Mohamed Abbas, principal investigator, Assiut University
ClinicalTrials.gov Identifier: NCT03178916     History of Changes
Other Study ID Numbers: BFHRP
First Submitted: June 6, 2017
First Posted: June 7, 2017
Last Update Posted: July 13, 2017
Last Verified: July 2017
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