Relationship Between Mechanical Ventilator's Modes , Intra-Abdominal Pressure, Mechanical Power and Gastric Tube Tolerance Among Mechanically Ventilated Patients.
MV and IAP
1 other identifier
observational
90
1 country
1
Brief Summary
The study aims to: Explore the relationship between MV modes on the IA, MP and GT tolerance among mechanically ventilated patients.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Aug 2026
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
June 23, 2026
CompletedFirst Posted
Study publicly available on registry
July 7, 2026
CompletedStudy Start
First participant enrolled
August 1, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 1, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
November 1, 2026
July 7, 2026
July 1, 2026
2 months
June 23, 2026
July 4, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
intra-abdominal pressure "IAP"
IAP will be measured through foly catheter
day 1
mechanical power
it will be: MP (J/ min) =0.098×RR×Vt × \[Peak Pressure-(DP/2)\] measured through folly catheter
day 1
gastric tube tolerance
The GT tolerance will be presented as yes if the patient was on GT feeding, and no, if the patient had delayed gastric emptying and converted to gastric drain
day 1
Study Arms (3)
SIMV group
this group are attached with MV on SIMV mode
CPAP group
this group are attached with MV on CPAP mode
BiPAP group
this group are attached with MV on BiPAP mode
Eligibility Criteria
A convenient sample
You may qualify if:
- adult patients requiring MV in ICU
You may not qualify if:
- patients with abdominal or chest trauma,
- patients with intra abdominal pathologies,
- patients who had received more than 10 units of red blood cells or more than 5 liters of intravenous liquids over the last 24 h,
- patients with sepsis or hepatic, or renal dysfunction,
- patients in positions other than supine, and
- body mass index (BMI) ≥ 30 kg/m2.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Faculty of Nursing, Damanhour University
Damanhūr, Egypt
Related Publications (1)
https://r.search.yahoo.com/_ylt=AwrFYna.5DpqRgIAKKRXNyoA;_ylu=Y29sbwNiZjEEcG9zAzEEdnRpZAMEc2VjA3Ny/RV=2/RE=1783454142/RO=10/RU=https%3a%2f%2fpmc.ncbi.nlm.nih.gov%2farticles%2fPMC3733186%2f/RK=2/RS=5S3GXdIx14M.h5tX6E6bTclSBZw-
BACKGROUND
Related Links
Study Officials
- PRINCIPAL INVESTIGATOR
sahar youness youness, professor
professor of emergency and critical nursing
Central Study Contacts
Alaa Mustafa assistant professor, assistant professor
CONTACT
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- PROSPECTIVE
- Target Duration
- 3 Days
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Faculty member " lecturer"
Study Record Dates
First Submitted
June 23, 2026
First Posted
July 7, 2026
Study Start
August 1, 2026
Primary Completion (Estimated)
October 1, 2026
Study Completion (Estimated)
November 1, 2026
Last Updated
July 7, 2026
Record last verified: 2026-07
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL
- Time Frame
- Octuber, 2026 and will be available for 5 years
- Access Criteria
- any researcher will be able to access
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