- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05544097
Spectral Analysis of Bowel Sounds in Preterm Babies of Less Than 32 Weeks of Amenorrhea (WA) as Predictive Factor of Enterocolitis (BHAPE)
July 9, 2024 updated by: Centre Hospitalier Universitaire, Amiens
The recording or bowels is easy and cheap.
The investigators wonder if these sounds are modified in babies with high risk of necrotizing enterocolitis.
In this study, the investigators suggest to record and do a spectral analysis of 30 seconds of bowel sounds in preterm babies of less than 32WA before and after enteral nutrition, every day until the end of hospitalization.
A spectral analysis will be made for each record to determine frequencies of the signal.
The investigators will try to determine physiological frequencies and look for modifications in pathological situations.
Study Overview
Status
Recruiting
Intervention / Treatment
Study Type
Interventional
Enrollment (Estimated)
50
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: André LOKOMBE-LEKE, DR
- Phone Number: 03 22 08 76 07
- Email: leke.andre@chu-amiens.fr
Study Locations
-
-
-
Amiens, France, 80000
- Recruiting
- CHU Amiens
-
Sub-Investigator:
- Pierre TOURNEUX, Pr
-
Sub-Investigator:
- François MOREAU, Dr
-
Contact:
- Andre Leke, MD
- Phone Number: (33)322087607
- Email: leke.andre@chu-amiens.fr
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
No older than 7 months (Child)
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- preterm babies of less than 32WA
Exclusion Criteria:
- preterm babies of more than 32WA,
- digestive congenital malformation
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
variation of spectral analysis of bowel sounds (frequency in Hz) before and after enteral nutrition
Time Frame: 36 months
|
establishing spectral analysis of bowel sounds
|
36 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
September 6, 2022
Primary Completion (Estimated)
November 1, 2025
Study Completion (Estimated)
November 1, 2025
Study Registration Dates
First Submitted
September 6, 2022
First Submitted That Met QC Criteria
September 15, 2022
First Posted (Actual)
September 16, 2022
Study Record Updates
Last Update Posted (Actual)
July 10, 2024
Last Update Submitted That Met QC Criteria
July 9, 2024
Last Verified
July 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Digestive System Diseases
- Pathologic Processes
- Gastrointestinal Diseases
- Gastroenteritis
- Intestinal Diseases
- Pregnancy Complications
- Obstetric Labor Complications
- Obstetric Labor, Premature
- Menstruation Disturbances
- Female Urogenital Diseases and Pregnancy Complications
- Urogenital Diseases
- Premature Birth
- Enterocolitis
- Enterocolitis, Necrotizing
- Amenorrhea
Other Study ID Numbers
- PI2019_843_0025
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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