Skip to content

Clinical study of tube administration speed of viscosity modifiered enteral fomula

Clinical study of tube administration speed of viscosity modifiered enteral fomula - tube administration speed of viscosity modifiered enteral fomula

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000016013
Enrollment
15
Registered
2015-01-05
Start date
2014-12-22
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Tube feeding

Interventions

The objects are administerd viscosity controlled enteral formula.

Sponsors

VF researching group
Lead Sponsor
Tanashi hospital, Clover hospital, ASAHI KASEI PHARMA CORPORATION
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: The patients who undergo tube feeding.The subject who recognized the examination and is able to give the agreement. The patients who is undergoing tube feeding with nasogastric catheter 5 days or longer.

Exclusion criteria

Exclusion criteria: The patients who are cirtified as contraindication case of this study by attending doctor. The patients out of indication for tube feeding. The patients have a complication durig the study.

Design outcomes

Primary

MeasureTime frame
Administration speed comparing with in vitro study

Secondary

MeasureTime frame
Change of urinal pH.change of body weight. Frequency of diarrhea and constipation. Change of body temparature. The room temparature.

Countries

Japan

Contacts

Public ContactNaohiro Washizawa

Toho University Omori Medical Center Nutrition Therapy Center

washi@med.toho-u.ac.jp03-3762-4151

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026