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The Australian Placental Transfusion Study (APTS): Should Very Pre Term Babies Receive a Placental Blood Transfusion at Birth Via Deferring Cord Clamping Versus Standard Cord Clamping Procedures?
NCT02606058 · View on ClinicalTrials.gov ↗
Study Summary
To establish if placental transfusion, using deferred cord clamping for 60 seconds or more while holding the baby at or below the level of the placenta, will improve survival without disability compared with standard early cord clamping in preterm babies less than 30 weeks of gestation.
Conditions Studied
Interventions
- PROCEDURE Deferred cord clamping
Study Locations (20)
New South Wales
- John Hunter Hospital — Newcastle
- Liverpool Hospital — Sydney
- Royal Prince Alfred Hospital — Sydney
- Royal North Shore Hospital — Sydney
- Royal Hospital for Women — Sydney
- Nepean Hospital — Sydney
Queensland
- Mater Mother's Hospital — Brisbane
- Royal Brisbane and Women's Hospital — Brisbane
- Townsville Hospital — Townsville
Other
- Hôpital Antoine-Béclère — Clamart
- Auckland Hospital — Auckland
- Christchurch Hospital — Christchurch
Victoria
- Monash Medical Centre — Melbourne
- Mercy Hospital for Women — Melbourne
Texas
- Baylor College of Medicine — Houston
Vermont
- University of Vermont Medical Centre — Burlington
Australian Capital Territory
- Canberra Hospital — Canberra
South Australia
- Flinders Medical Centre — Adelaide
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 1,637 participants |
| Start Date | 2010-09 |
| Est. Completion | 2020-09 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02606058
The ClinicalTrials.gov registry entry for NCT02606058 describes a study currently listed as completed. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 1,637 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Sydney, which has 6 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Preterm Birth appearing as the primary indexed condition, and to 1 intervention — of which Deferred cord clamping is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT02606058 reports 20 study locations spanning 10 distinct geographic areas — top geographies include New South Wales, Queensland, Other. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT02606058 about?
NCT02606058 is a clinical study titled "The Australian Placental Transfusion Study (APTS): Should Very Pre Term Babies Receive a Placental Blood Transfusion at Birth Via Deferring Cord Clamping Versus Standard Cord Clamping Procedures?". To establish if placental transfusion, using deferred cord clamping for 60 seconds or more while holding the baby at or below the level of the placenta, will improve survival without disability compared with standard early cord clamping in preterm babies less than 30 weeks of gestation.
What is the current status of trial NCT02606058?
This trial is currently completed. It is a NA study. The enrollment target is 1,637 participants. The study started on 2010-09. Estimated completion is 2020-09.
What conditions does trial NCT02606058 study?
This clinical trial studies the following conditions: Preterm Birth. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT02606058?
The interventions under investigation include: Deferred cord clamping (PROCEDURE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT02606058?
This trial is sponsored by University of Sydney, which has 6 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT02606058 being conducted?
This trial has 20 study locations across Texas, Vermont, Australian Capital Territory, New South Wales, Queensland. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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