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Trial · NCT01860014

Comparison of Two Different Natural Surfactants in the Treatment of Pulmonary Hemorrhage

NCT01860014, Not applicable, Completed, Dr. Sami Ulus Children's Hospital

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Comparison of Two Different Natural Surfactants in the Treatment of Pulmonary Hemorrhage. Trials, record NCT01860014. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT01860014

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Trial

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

Title
Comparison of Two Different Natural Surfactants in the Treatment of Pulmonary Hemorrhage
NCT number
NCT01860014
Status
Completed
Phases
Not applicable
Enrollment
20 participants, actual
Lead sponsor
Dr. Sami Ulus Children's Hospital
Conditions
Pulmonary Hemorrhage
Interventions
Poractant alfa, Beractant
First posted
2013-05-22
Last updated
2013-05-22

Source ClinicalTrials.gov

Registered outcomes2

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

ListOutcomeTime frameDescription
PrimaryOxygen requirement6 hourWe will evaluate the need of oxygen support within 6 hour after surfactant
SecondaryMortality4 weeksWe will compare the rate of mortality between the groups during neonatal period

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.

Papers1

The papers the trial lists on ClinicalTrials.gov.

PMIDListed as
8095608RESULT

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 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.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

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/NCT01860014

GET https://conductscience.org/api/trials/v1/NCT01860014/registered