Trial · NCT02512224

Comparison of Outcomes Between Parenteral and Enteral Nutrition

NCT02512224, Completed, Tokyo University; results first posted 2015-09-10

3 sourcestrials-2026-11-12-0.4.0

Cite this record

ConductScience Library. Comparison of Outcomes Between Parenteral and Enteral Nutrition. Trials, record NCT02512224. Release trials-2026-11-12-0.4.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT02512224

On this page

Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title: Comparison of Outcomes Between Parenteral and Enteral Nutrition
NCT number: NCT02512224
Status: Completed
Enrollment: 5,824 participants, actual
Lead sponsor: Tokyo University
Conditions: Deglutition Disorders
Interventions: Parenteral nutrition, Enteral nutrition
First posted: 2015-07-30
Last updated: 2015-09-30
Results first posted: 2015-09-10

Source ClinicalTrials.gov

Registered outcomes6

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

List	Outcome	Time frame
Primary	Mortality Calculated From Outcome Section From DPC Database at 90 Days	90 days after the start of the procedure
Secondary	Post-procedural Pneumonia	the incidence of post-procedural pneumonia occurring during hospitalization. Participants will be followed for the duration of hospital stay, an expected median of 3 weeks after procedure.
Secondary	Post-procedural Sepsis	the incidence of post-procedural sepsis occurring during hospitalization. Participants will be followed for the duration of hospital stay, an expected median of 3 weeks after procedure.
Secondary	Re-admission 30 Days	re-admission within 30 days of discharge.
Secondary	Mortality Calculated From Outcome Section From DPC Database at 14 Days	14 days after the start of the procedure
Secondary	Mortality Calculated From Outcome Section From DPC Database at 30 Days	30 days after the start of the procedure

Source ClinicalTrials.gov

Outcomes6

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

Type	Outcome	Time frame	Units	Measured as
PRIMARY	Mortality Calculated From Outcome Section From DPC Database at 90 Days	90 days after the start of the procedure	Participants	NUMBER
SECONDARY	Post-procedural Pneumonia	the incidence of post-procedural pneumonia occurring during hospitalization. Participants will be followed for the duration of hospital stay, an expected median of 3 weeks after procedure.	Participants	NUMBER
SECONDARY	Post-procedural Sepsis	the incidence of post-procedural sepsis occurring during hospitalization. Participants will be followed for the duration of hospital stay, an expected median of 3 weeks after procedure.	Participants	NUMBER
SECONDARY	Re-admission 30 Days	re-admission within 30 days of discharge.	Participants	NUMBER
SECONDARY	Mortality Calculated From Outcome Section From DPC Database at 14 Days	14 days after the start of the procedure	Participants	NUMBER
SECONDARY	Mortality Calculated From Outcome Section From DPC Database at 30 Days	30 days after the start of the procedure	participants	NUMBER

Source ClinicalTrials.gov

Results by group12

Each measurement the trial posted, group by group, in the words and numbers it posted.

Outcome	Group	Value	Units
Mortality Calculated From Outcome Section From DPC Database at 90 Days	Parenteral Nutrition	359	Participants
Mortality Calculated From Outcome Section From DPC Database at 90 Days	Enteral Nutrition	287	Participants
Post-procedural Pneumonia	Parenteral Nutrition	346	Participants
Post-procedural Pneumonia	Enteral Nutrition	450	Participants
Post-procedural Sepsis	Parenteral Nutrition	129	Participants
Post-procedural Sepsis	Enteral Nutrition	108	Participants
Re-admission 30 Days	Parenteral Nutrition	188	Participants
Re-admission 30 Days	Enteral Nutrition	159	Participants
Mortality Calculated From Outcome Section From DPC Database at 14 Days	Parenteral Nutrition	114	Participants
Mortality Calculated From Outcome Section From DPC Database at 14 Days	Enteral Nutrition	89	Participants

1 to 10 of 12Source ClinicalTrials.gov

See all 12 results by group

Participant flow6

How many started, completed or left each group, period by period.

Period	Milestone	Group	Participants
Overall Study	STARTED	Parenteral Nutrition	2,912
Overall Study	STARTED	Enteral Nutrition	2,912
Overall Study	COMPLETED	Parenteral Nutrition	2,912
Overall Study	COMPLETED	Enteral Nutrition	2,912
Overall Study	NOT COMPLETED	Parenteral Nutrition	0
Overall Study	NOT COMPLETED	Enteral Nutrition	0

Source ClinicalTrials.gov

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals6

The totals the trial posted for each group.

Total	Group	Affected	At risk
Total, all-cause mortality	Parenteral Nutrition
Total, all-cause mortality	Enteral Nutrition
Total, other adverse events	Parenteral Nutrition	0	2,912
Total, other adverse events	Enteral Nutrition	0	2,912
Total, serious adverse events	Parenteral Nutrition	0	2,912
Total, serious adverse events	Enteral Nutrition	0	2,912

Source ClinicalTrials.gov

Papers1

The papers the trial lists on ClinicalTrials.gov.

PMID	Listed as
26447149	DERIVED

Source PubMed

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons7

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

Comparison	Source
Parenteral Nutrition vs Enteral Nutrition: Mortality Calculated From Outcome Section From DPC Database at 90 Days	Trial comparisons
Parenteral Nutrition vs Enteral Nutrition: Post-procedural Pneumonia	Trial comparisons
Parenteral Nutrition vs Enteral Nutrition: Re-admission 30 Days	Trial comparisons
Parenteral Nutrition vs Enteral Nutrition: Post-procedural Sepsis	Trial comparisons
Parenteral Nutrition vs Enteral Nutrition: Mortality Calculated From Outcome Section From DPC Database at 30 Days	Trial comparisons
Parenteral Nutrition vs Enteral Nutrition: Mortality Calculated From Outcome Section From DPC Database at 14 Days	Trial comparisons
Parenteral Nutrition vs Enteral Nutrition: serious adverse events	Trial comparisons

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Source

Release: trials-2026-11-12-0.4.0
Release manifest SHA-256: 0f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4
Registry capture: 2026-11-12
Results copy, AACT: 2026-03-23
NIH clinical studies file: 2026-11-13

Source ClinicalTrials.gov

Sources 3

ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
ClinicalTrials.govNone stated
NIH RePORTER's clinical studies and project filesPublic domain

Each source's terms

ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
ClinicalTrials.govnone stated
NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT02512224

GET https://conductscience.org/api/trials/v1/NCT02512224/registered

API reference For AI assistants