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Trial · NCT04696003

Treatment of Classic Mid-trimester PPROM by Means of Continuous Amnioinfusion

NCT04696003, Phase 3, Unknown, Martin-Luther-Universität Halle-Wittenberg

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Treatment of Classic Mid-trimester PPROM by Means of Continuous Amnioinfusion. Trials, record NCT04696003. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT04696003

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Trial

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

Title
Treatment of Classic Mid-trimester PPROM by Means of Continuous Amnioinfusion
NCT number
NCT04696003
Status
Unknown
Phases
Phase 3
Enrollment
68 participants, estimated
Lead sponsor
Martin-Luther-Universität Halle-Wittenberg
Conditions
Bronchopulmonary Dysplasia, Necrotizing Enterocolitis, Intracranial Hemorrhages
Interventions
Continuous amnioinfusion with Amnion Flush Solution through the intraamniotic catheter
First posted
2021-01-06
Last updated
2021-01-12

Source ClinicalTrials.gov

Registered outcomes6

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

ListOutcomeTime frameDescription
PrimaryNumber of Participants with bronchopulmonary dysplasiathrough study completion, an average of 1 yearNumber of Participants with severe bronchopulmonary dysplasia (BPD)
PrimaryNumber of Participants with intraventricular hemorrhagethrough study completion, an average of 1 yearNumber of Participants with intraventricular hemorrhage (IVH 3-4)
PrimaryNumber of Participants with necrotizing enterocolitisthrough study completion, an average of 1 yearNumber of Participants with necrotizing enterocolitis (NEC)
SecondaryDuration of PPROM to delivery intervalup to 15 weeksDuration of PPROM to delivbery interval (days)
SecondaryGesatational age at delivery34 weeksgestational age at delivery
SecondaryRate of Newborns with FIRS1 weekRate of Newborns with FIRS (fetal inflammatory response syndrome) (binary)

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.

Papers4

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
23774012BACKGROUNDPubMed
26447923BACKGROUNDPubMed
28710882RESULTPubMed
36143388DERIVEDPubMed

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/NCT04696003

GET https://conductscience.org/api/trials/v1/NCT04696003/registered