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NCT02272387 · ClinicalTrials.gov registry record · NA
Is Vitamin D Insufficiency and Deficiency Associated With Antepartum and Postpartum Depression?
A NA study, sponsored by St. Luke's-Roosevelt Hospital Center.
- Terminated
- Registry status
- NA
- Development phase
- 151
- Enrollment target
NCT02272387 is a NA study that was terminated before completion, run by St. Luke's-Roosevelt Hospital Center. The registered enrollment target is 151 participants.
The verdict
NCT02272387, a NA study, was terminated before completion, sponsored by St. Luke's-Roosevelt Hospital Center.
- TERMINATED
- Registry status
- NA
- Development phase
- 151 participants
- Enrollment target
Study Summary
Our primary aim is to evaluate whether Vitamin D deficiency causes depressive symptoms in antepartum and postpartum depression and whether early correction of Vitamin D deficiency improves these symptoms. Our secondary aims evaluate maternal and fetal outcomes including antepartum, intrapartum, and immediate postpartum complications. We are also evaluating the effectiveness of a common vitamin D treatment regimen used outside of pregnancy.
Interventions
- OTHER Placebo
- DIETARY_SUPPLEMENT Vitamin D3 (Cholecalciferol)
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 151 participants |
| Start Date | 2014-10 |
| Est. Completion | 2016-04-14 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02272387
The ClinicalTrials.gov registry entry for NCT02272387 describes a study currently listed as terminated, categorized as NA. The registered enrollment target is 151 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is St. Luke's-Roosevelt Hospital Center, which has 57 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.
NCT02272387 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT02272387 about?
NCT02272387 is a clinical study titled "Is Vitamin D Insufficiency and Deficiency Associated With Antepartum and Postpartum Depression?". Our primary aim is to evaluate whether Vitamin D deficiency causes depressive symptoms in antepartum and postpartum depression and whether early correction of Vitamin D deficiency improves these symptoms. Our secondary aims evaluate maternal and fetal outcomes including antepartum, intrapartum, and...
What is the current status of trial NCT02272387?
This trial is currently terminated. It is a NA study. The enrollment target is 151 participants. The study started on 2014-10. Estimated completion is 2016-04-14.
What interventions are being tested in trial NCT02272387?
The interventions under investigation include: Placebo (OTHER), Vitamin D3 (Cholecalciferol) (DIETARY_SUPPLEMENT).
Who is sponsoring clinical trial NCT02272387?
This trial is sponsored by St. Luke's-Roosevelt Hospital Center, which has 57 total clinical trials registered on ClinicalTrials.gov.
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