Trial · NCT01802099
Impact of Early Enteral vs. Parenteral Nutrition on Mortality in Patients Requiring Mechanical Ventilation and Catecholamines
NCT01802099, Not applicable, Completed, Centre Hospitalier Departemental Vendee; results first posted 2026-01-22
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Impact of Early Enteral vs. Parenteral Nutrition on Mortality in Patients Requiring Mechanical Ventilation and Catecholamines. Trials, record NCT01802099. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT01802099
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Impact of Early Enteral vs. Parenteral Nutrition on Mortality in Patients Requiring Mechanical Ventilation and Catecholamines
- NCT number
- NCT01802099
- Status
- Completed
- Phases
- Not applicable
- Enrollment
- 2,410 participants, actual
- Lead sponsor
- Centre Hospitalier Departemental Vendee
- Conditions
- Acute Respiratory Failure, Shock
- Interventions
- Enteral nutrition, Parenteral nutrition
- First posted
- 2013-03-01
- Last updated
- 2026-09-04
- Results first posted
- 2026-01-22
Source ClinicalTrials.gov
Registered outcomes14
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Mortality | 28 days | |
| Secondary | Mortality Rate | 90 days | |
| Secondary | Ventilator-associated Pneumonia Rate | until weaning of mechanical ventilation (average: 7 days) | |
| Secondary | Nosocomial Infections Rate | until discharge from ICU (average: 10 days) | Bloodstream infection Urinary tract infection Catheter-related infection Other infections |
| Secondary | Length of Stay in Intensive Care Unit (ICU) | until discharge from ICU (average: 10 days) | |
| Secondary | Length of Stay in Hospital | until discharge from hospital (average: 17 days) | |
| Secondary | Variations in Sepsis-related Organ Failure Assessment (SOFA) Score | first week (7 days) of mechanical ventilation | |
| Secondary | Calories Intake | until weaning of mechanical ventilation (average : 7 days) | |
| Secondary | Proportion of Patients Given 100% of the Calorie Target | until weaning of mechanical ventilation (average: 7 days) | |
| Secondary | Cumulative Calorie Deficit From Day 0 to Day 7 | During the first week (7 days) of mechanical ventilation |
1 to 10 of 14Source ClinicalTrials.gov
See all 14 registered outcomesOutcomes14
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
| Type | Outcome | Time frame | Population | Units | Measured as |
|---|---|---|---|---|---|
| PRIMARY | Mortality | 28 days | Participants | COUNT_OF_PARTICIPANTS | |
| SECONDARY | Mortality Rate | 90 days | |||
| SECONDARY | Ventilator-associated Pneumonia Rate | until weaning of mechanical ventilation (average: 7 days) | |||
| SECONDARY | Nosocomial Infections Rate | until discharge from ICU (average: 10 days) | |||
| SECONDARY | Length of Stay in Intensive Care Unit (ICU) | until discharge from ICU (average: 10 days) | |||
| SECONDARY | Length of Stay in Hospital | until discharge from hospital (average: 17 days) | |||
| SECONDARY | Variations in Sepsis-related Organ Failure Assessment (SOFA) Score | first week (7 days) of mechanical ventilation | |||
| SECONDARY | Calories Intake | until weaning of mechanical ventilation (average : 7 days) | |||
| SECONDARY | Proportion of Patients Given 100% of the Calorie Target | until weaning of mechanical ventilation (average: 7 days) | |||
| SECONDARY | Cumulative Calorie Deficit From Day 0 to Day 7 | During the first week (7 days) of mechanical ventilation |
1 to 10 of 14Source ClinicalTrials.gov
See all 14 outcomesResults by group2
Each measurement the trial posted, group by group, in the words and numbers it posted.
| Outcome | Group | Category | Value | Spread | Units |
|---|---|---|---|---|---|
| Mortality | Parenteral Nutrition | 422 | Participants | ||
| Mortality | Enteral Nutrition | 443 | Participants |
Source ClinicalTrials.gov
Participant flow6
How many started, completed or left each group, period by period.
| Period | Milestone | Group | Participants | Units counted |
|---|---|---|---|---|
| Overall Study | STARTED | Parenteral Nutrition | 1,208 | |
| Overall Study | STARTED | Enteral Nutrition | 1,202 | |
| Overall Study | COMPLETED | Parenteral Nutrition | 1,208 | |
| Overall Study | COMPLETED | Enteral Nutrition | 1,202 | |
| 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 | 1,208 |
| Total, other adverse events | Enteral Nutrition | 0 | 1,202 |
| Total, serious adverse events | Parenteral Nutrition | 0 | 1,208 |
| Total, serious adverse events | Enteral Nutrition | 0 | 1,202 |
Source ClinicalTrials.gov
Papers2
The papers the trial lists on ClinicalTrials.gov.
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 comparisons2
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
| Comparison | Source |
|---|---|
| Parenteral Nutrition vs Enteral Nutrition: Mortality | 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.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license 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/NCT01802099
GET https://conductscience.org/api/trials/v1/NCT01802099/registered