Effect of Enteral Feeding on Paraclinical Outcome

Phase 3

• Conditions: Paraclinical changes in continuous feeding and bolus feeding.

• Registration Number: IRCT20190128042528N1
• Lead Sponsor: Tehran University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 24 February 2020

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 34

Inclusion Criteria

Patient with mechanical ventilation throught the endotracheal tube
Feeding of Patient with NG tube
Patient attendant satisfaction
18-85 years old

Exclusion Criteria

Patient with digestive Disease( diarrhea, ileus, obstruction, ostomy)
Patient with renal failure

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Serum albumin level. Timepoint: Before the intervention and 7 days after the intervention. Method of measurement: Analysis by Bromocresol Green Pars Test Laboratory Kit.;Serum level of pre-albumin. Timepoint: Before the intervention and 2 days after the intervention. Method of measurement: Analysis by Nephlometry Laboratory Kit Brand Binding site.;Serum phosphate level. Timepoint: Before the intervention and 7 days after the intervention. Method of measurement: Photometric analysis uv test.;Serum lactate level. Timepoint: Before the intervention and 7 days after the intervention. Method of measurement: Enzymatic / colorimetric analysis kit by Fars Bayer Lab.;Frequency of defecation. Timepoint: During 7 days of intervention. Method of measurement: View and record in data log sheet.;Patient's blood sugar. Timepoint: Every six hours. Method of measurement: clever check Glucometer.