Trial · NCT01187225
Fibrinogen Concentrate In Children After Cardiac Surgery
NCT01187225, Phase 2, Completed, University of Sao Paulo
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Fibrinogen Concentrate In Children After Cardiac Surgery. Trials, record NCT01187225. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT01187225
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Fibrinogen Concentrate In Children After Cardiac Surgery
- NCT number
- NCT01187225
- Status
- Completed
- Phases
- Phase 2
- Enrollment
- 63 participants, actual
- Lead sponsor
- University of Sao Paulo
- Conditions
- Cardiac Surgical Procedures, Blood Coagulation Disorders, Fibrinogen, Cryoprecipitate
- Interventions
- Fibrinogen concentrate, Cryoprecipitate
- First posted
- 2010-08-24
- Last updated
- 2013-01-04
Source ClinicalTrials.gov
Registered outcomes8
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Number of patients receiving any allogeneic blood products | From ICU admission until hospital discharge | Percentage of patients exposed to allogeneic blood products (red blood cells, FFP, platelet concentrate and cryoprecipitate) after ICU admission until hospital discharge. |
| Secondary | Length of ICU stay | Up to ICU discharge | Length of ICU stay - days since arrival at ICU until discharge |
| Secondary | Clinical complications - renal failure, respiratory failure,sepsis, myocardial ischemia, stroke | Up to hospital discharge | Clinical complications since intraoperative until hospital discharge |
| Secondary | Mechanical ventilation free-days | Up to ICU discharge | Number of days without mechanical ventilation during ICU stay |
| Secondary | Length of hospital stay | Up to hospital discharge | Number of days since arrival at ICU until hospital discharge |
| Secondary | Vasopressors free-days | Up to ICU discharge | Number of days without vasopressors during ICU stay |
| Secondary | intraoperative transfusion | intraoperative period | intraoperative requirements of any blood product (red blood cells, FFP, platelet concentrate and cryoprecipitate)) |
| Secondary | postoperative blood losses | from ICU admission until hospital discharge | postoperative blood losses determined by the weight of dressings at intraoperative and chest tube drainage 12h and 24h after ICU admission |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
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 totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
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 comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
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/NCT01187225
GET https://conductscience.org/api/trials/v1/NCT01187225/registered