Trial · NCT01002482
Computerized Glucose Control in Critically Ill Patients
NCT01002482, Phase 3, Completed, Centre Hospitalier of Chartres; results first posted 2013-12-03
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Computerized Glucose Control in Critically Ill Patients. Trials, record NCT01002482. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT01002482
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Computerized Glucose Control in Critically Ill Patients
- NCT number
- NCT01002482
- Status
- Completed
- Phases
- Phase 3
- Enrollment
- 2,684 participants, actual
- Lead sponsor
- Centre Hospitalier of Chartres
- Conditions
- Hyperglycemia, Critical Illness
- Interventions
- CGAO-based Glucose Control, Standard-Care Glucose Control
- First posted
- 2009-10-27
- Last updated
- 2013-12-03
- Results first posted
- 2013-12-03
Source ClinicalTrials.gov
Registered outcomes10
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | All-cause 90-day Mortality | Day 90 | |
| Secondary | All-cause 28-day Mortality | Day 28 | |
| Secondary | All-cause Intensive Care Unit Mortality | Date of discharge from the ICU | |
| Secondary | All-cause In-hospital Mortality | Day of discharge from the hospital | |
| Secondary | Intensive Care Unit Free Days | 28 days | Intensive care unit free days was 28-day-ICU-free-days i.e. was calculated by subtracting the actual ICU duration in days from 28 with patients who died at day 28 or before being assigned 0 free-days and those who had a stay in ICU of 28 days or more being also assigned 0 free-days |
| Secondary | Time Spent in Blood Glucose Target | Day of discharge from the ICU | |
| Secondary | Severe Hypoglycemia | Date of discharge from the ICU | Number of patients with severe biological hypoglycemia (defined as blood glucose of 40 mg per deciliter or less)regardless of clinical signs |
| Secondary | Hospital Length of Stay | Date of discharge from the hospital | |
| Secondary | Intensive Care Unit Length of Stay | Date of discharge from the ICU | |
| Secondary | Incidence of Nosocomial Bacteriemia | Date of discharge from the ICU |
Source ClinicalTrials.gov
Outcomes10
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
| Type | Outcome | Time frame | Population | Units | Measured as |
|---|---|---|---|---|---|
| PRIMARY | All-cause 90-day Mortality | Day 90 | participants | NUMBER | |
| SECONDARY | All-cause 28-day Mortality | Day 28 | participants | NUMBER | |
| SECONDARY | All-cause Intensive Care Unit Mortality | Date of discharge from the ICU | participants | NUMBER | |
| SECONDARY | All-cause In-hospital Mortality | Day of discharge from the hospital | participants | NUMBER | |
| SECONDARY | Intensive Care Unit Free Days | 28 days | days | MEDIAN | |
| SECONDARY | Time Spent in Blood Glucose Target | Day of discharge from the ICU | |||
| SECONDARY | Severe Hypoglycemia | Date of discharge from the ICU | participants | NUMBER | |
| SECONDARY | Hospital Length of Stay | Date of discharge from the hospital | days | MEDIAN | |
| SECONDARY | Intensive Care Unit Length of Stay | Date of discharge from the ICU | days | MEDIAN | |
| SECONDARY | Incidence of Nosocomial Bacteriemia | Date of discharge from the ICU |
Source ClinicalTrials.gov
Results by group16
Each measurement the trial posted, group by group, in the words and numbers it posted.
| Outcome | Group | Category | Value | Spread | Units |
|---|---|---|---|---|---|
| All-cause 90-day Mortality | CGAO-based Glucose Control | 431 | participants | ||
| All-cause 90-day Mortality | Standard-Care Glucose Gontrol | 447 | participants | ||
| All-cause 28-day Mortality | CGAO-based Glucose Control | 326 | participants | ||
| All-cause 28-day Mortality | Standard-Care Glucose Gontrol | 328 | participants | ||
| All-cause Intensive Care Unit Mortality | CGAO-based Glucose Control | 302 | participants | ||
| All-cause Intensive Care Unit Mortality | Standard-Care Glucose Gontrol | 310 | participants | ||
| All-cause In-hospital Mortality | CGAO-based Glucose Control | 376 | participants | ||
| All-cause In-hospital Mortality | Standard-Care Glucose Gontrol | 393 | participants | ||
| Intensive Care Unit Free Days | CGAO-based Glucose Control | 14 | Inter-Quartile Range 0 to 22 | days | |
| Intensive Care Unit Free Days | Standard-Care Glucose Gontrol | 13 | Inter-Quartile Range 0 to 23 | days |
1 to 10 of 16Source ClinicalTrials.gov
See all 16 results by groupParticipant flow6
How many started, completed or left each group, period by period.
| Period | Milestone | Group | Participants | Units counted |
|---|---|---|---|---|
| Overall Study | STARTED | CGAO-based Glucose Control | 1,351 | |
| Overall Study | STARTED | Standard-Care Glucose Gontrol | 1,333 | |
| Overall Study | COMPLETED | CGAO-based Glucose Control | 1,336 | |
| Overall Study | COMPLETED | Standard-Care Glucose Gontrol | 1,312 | |
| Overall Study | NOT COMPLETED | CGAO-based Glucose Control | 15 | |
| Overall Study | NOT COMPLETED | Standard-Care Glucose Gontrol | 21 |
Source ClinicalTrials.gov
Adverse events2
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
| Type | Event | Organ system | Group | Affected | At risk | Events |
|---|---|---|---|---|---|---|
| serious | BG of 40 mg per deciliter or less accompanied with observed or suspected neurological symptoms | Metabolism and nutrition disorders | CGAO-based Glucose Control | 20 | 1,336 | 23 |
| serious | BG of 40 mg per deciliter or less accompanied with observed or suspected neurological symptoms | Metabolism and nutrition disorders | Standard-Care Glucose Gontrol | 6 | 1,312 | 9 |
Source ClinicalTrials.gov
Adverse event totals6
The totals the trial posted for each group.
| Total | Group | Affected | At risk |
|---|---|---|---|
| Total, all-cause mortality | CGAO-based Glucose Control | ||
| Total, all-cause mortality | Standard-Care Glucose Gontrol | ||
| Total, other adverse events | CGAO-based Glucose Control | 0 | 1,336 |
| Total, other adverse events | Standard-Care Glucose Gontrol | 0 | 1,312 |
| Total, serious adverse events | CGAO-based Glucose Control | 20 | 1,336 |
| Total, serious adverse events | Standard-Care Glucose Gontrol | 6 | 1,312 |
Source ClinicalTrials.gov
Papers4
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 comparisons6
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
| Comparison | Source |
|---|---|
| CGAO-based Glucose Control vs Standard-Care Glucose Gontrol: All-cause In-hospital Mortality | Trial comparisons |
| CGAO-based Glucose Control vs Standard-Care Glucose Gontrol: All-cause 28-day Mortality | Trial comparisons |
| CGAO-based Glucose Control vs Standard-Care Glucose Gontrol: Severe Hypoglycemia | Trial comparisons |
| CGAO-based Glucose Control vs Standard-Care Glucose Gontrol: All-cause 90-day Mortality | Trial comparisons |
| CGAO-based Glucose Control vs Standard-Care Glucose Gontrol: All-cause Intensive Care Unit Mortality | Trial comparisons |
| CGAO-based Glucose Control vs Standard-Care Glucose Gontrol: 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/NCT01002482
GET https://conductscience.org/api/trials/v1/NCT01002482/registered