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Comparative study of bolus and intermittent tube feeding

Comparative study of bolus and intermittent tube feeding impacts on intolerance nutrition and respiratory aspiration among sepsis patients in intensive care unit

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015102623446N2
Enrollment
Unknown
Registered
2016-03-25
Start date
2015-10-23
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

sepsis. Streptococcal sepsis, Other sepsis

Interventions

Intervention 1: Intervention group 1:bolus feeding. The gavage will be performed gently using a syringe within 15-60 minutes depending on the condition and required volume. Intervention 2: interventio
Intervention group 1:bolus feeding. The gavage will be performed gently using a syringe within 15-60 minutes depending on the condition and required volume.
intervention group 2: intermittent. The intermittent nutrition using the pump for at least 4 and up to 20 hours depending on the conditions and required volume.
control group: In the control group routine procedure in the ICU for fed carried out.

Sponsors

Vice chancellor for research, Aja University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: aged between18 to 65 years old; admitted to the intensive care units diagnosed with sepsis? the level of consciousness of less than 10; inability to eat through oral way and compelling need to nutritional support; lack of digestive disorders after confirming ICU physician; intubated the patient. Exclusion criteria: increasing level of consciousness and develop the ability to eat during the study; discharge from ICU 10 days before admission; hemodynamic disorders and the need for new therapeutic intervention; signs of dehydration; addiction? receiving proton pump inhibitors; the need for a change in diet and the need to prescribe a specific diet during the study.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Diarrhea. Timepoint: Three Days. Method of measurement: Check List.;Constipation. Timepoint: Three Days. Method of measurement: Check List.;Puke. Timepoint: Three Days. Method of measurement: Check List.;Residual Volume. Timepoint: Three Days. Method of measurement: Check List.;Abdomen Stretch. Timepoint: Three Days. Method of measurement: Check List.

Secondary

MeasureTime frame
Aspirsion. Timepoint: Three. Method of measurement: Chck List.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactShahla Aliyari

AJA University of Medical Sciences

z.farsi@ajaums.ac.ir+98 217750040400

Outcome results

None listed

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