Trial · NCT00413946
Does Erythropoietin Improve Outcome in Very Preterm Infants?
NCT00413946, Phase 2, Completed, Swiss Neonatal Network
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Does Erythropoietin Improve Outcome in Very Preterm Infants? Trials, record NCT00413946. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT00413946
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Does Erythropoietin Improve Outcome in Very Preterm Infants?
- NCT number
- NCT00413946
- Status
- Completed
- Phases
- Phase 2
- Enrollment
- 420 participants, actual
- Lead sponsor
- Swiss Neonatal Network
- Conditions
- Intracranial Hemorrhage, Periventricular Leukomalacia, Cerebral Palsy, Developmental Psychomotor Disorders
- Interventions
- Recombinant human Erythropoietin, saline
- First posted
- 2006-12-20
- Last updated
- 2018-10-30
Source ClinicalTrials.gov
Registered outcomes4
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Mental developmental index (Bayley II) and motor, visual and hearing impairment | at age of 24 months corrected for prematurity. | |
| Secondary | MRI at term equivalent | 40 postmenstrual weeks | White matter injury score grey matter injury score brain maturation |
| Secondary | cerebral palsy. | First 24 months of life (corrected for prematurity) | |
| Secondary | Cognitive development and cerebral palsy | 5 years | Kaufmann ABC II, standardized neurological, visual and hearing examination, questionnaire about health status and behavior. Classification of impairments, disabilities and handicaps. |
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.
Papers8
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 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/NCT00413946
GET https://conductscience.org/api/trials/v1/NCT00413946/registered