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Comparison the efficiency of nutrition with entera meal and Ensure and standard gavage of hospital in traumatic patients

Comparison the efficiency of nutrition with entera meal standard formula and Ensure and standard gavage of hospital in traumatic patients at ICU in Vali-Asr hospital, Arak.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180112038319N1
Enrollment
66
Registered
2018-10-27
Start date
2018-10-22
Completion date
Unknown
Last updated
2019-01-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

traumatic patients. Unspecified early complication of trauma

Interventions

Intervention 1: First intervention group: Entera meal standard formula _ Dose and number of times is due to nutritional need of each patient. Duration of use is 14 days for each patient. Intervention

Sponsors

Arak University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: Age 18 to 50 Need to Nutrition with NG tube or Gastrostomy or Jejunostomy Multiple trauma

Exclusion criteria

Exclusion criteria: Death Gavage intolerance for more than 24 hours Patient re-NPO for more than 24 hours Reaction to Folate History of DM, hyper or hypothyroidism and metabolic disease Sensitivity to milk protein Gastro-intestinal fistula Burning Renal failure Hepatic failure

Design outcomes

Primary

MeasureTime frame
Serum total protein level: Serum albumin and globulin measurement. Timepoint: Serum total protein measurement at the beginning of trial(first day) and 8 and 14 days after Formula beginning. Method of measurement: Blood test.;Mid arm circumflex. Timepoint: Mid arm circumflex measurement at the beginning of trial(first day) and 8 and 14 days after Formula beginning. Method of measurement: non-stretchable tape measure.;Serum electrolytes: (Na, K, Ca, Mg). Timepoint: Serum electrolytes measurement at the beginning of trial(first day) and 8 and 14 days after Formula beginning. Method of measurement: Blood serum test.;NUTRIC score: This factor is designed to quantify the risk of critically ill patients developing adverse events at ICU. It determined with the table(age_APACHE score_SOFA score_ number of co-morbidities_days from hospital to ICU admission). Timepoint: NUTRIC score determination at the beginning of trial(first day) and 8 and 14 days after Formula beginning. Method of measurement: NUTRIC score table.

Secondary

MeasureTime frame
Side effect: diarrhea/Vomiting/Sensitivity. Timepoint: Complication incidence at the beginning of trial(first day) and 8 and 14 days after Formula beginning. Method of measurement: Patient physical examination.;Final price of each formula. Timepoint: end of fourteenth day. Method of measurement: Calculation the price of formula.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactShima Shahri

Arak University of Medical Sciences

sh.shahri@arakmu.ac.ir+98 86 3221 8317

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026