Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT02990988 · ClinicalTrials.gov registry record

Microbiome of Donor Iron Deficient Study

A clinical trial, sponsored by Columbia University.

Completed
Registry status
70
Enrollment target

NCT02990988: Completed study, sponsored by Columbia University.

NCT02990988 is a clinical trial that has completed, run by Columbia University. The registered enrollment target is 70 participants. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT02990988 has completed, sponsored by Columbia University.

COMPLETED
Registry status
70 participants
Enrollment target

Study Summary

The goal of this pilot study is to test whether the microbiome is affected by intravenous iron repletion.

Primary Outcome

Stool samples will be collected and processed.

Trial Details

FieldValue
Enrollment Target 70 participants
Start Date 2017-01
Est. Completion 2022-06-03
Columbia University

958 total trials

What the finished NCT02990988 record still lists

NCT02990988 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 70 participants, a relatively small participant target.

The record links to 0 conditions, and to 0 interventions.

NCT02990988 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02990988 about?

NCT02990988 is a clinical study titled "Microbiome of Donor Iron Deficient Study". The goal of this pilot study is to test whether the microbiome is affected by intravenous iron repletion.

What is the current status of trial NCT02990988?

This trial is currently completed. The enrollment target is 70 participants. The study started on 2017-01. Estimated completion is 2022-06-03.

Who is sponsoring clinical trial NCT02990988?

This trial is sponsored by Columbia University, which has 958 total clinical trials registered on ClinicalTrials.gov.

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT00969111 · 70 participants · NA

    Postoperative or Salvage Radiotherapy (RT) for Node Negative Prostate Cancer Following Radical Prostatectomy

  • NCT01712620 · 70 participants · Phase 2

    Spironolactone for Pulmonary Arterial Hypertension

  • NCT02143830 · 70 participants · Phase 2

    HSCT for Patients With Fanconi Anemia Using Risk-Adjusted Chemotherapy

  • NCT02601339 · 70 participants

    NIRS Monitoring in Premature Infants

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT02990988, the US trial registry maintained by the National Library of Medicine. NCT02990988 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.