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NCT01328704 · ClinicalTrials.gov registry record

Evaluate the Change in Iron, Vitamin D, and C-Reactive Protein Level (CRP) in a 12 to 24 Week Period

A clinical trial of Anemia and Vitamin D Deficiency, sponsored by Avera McKennan Hospital & University Health Center.

Completed
Registry status
50
Enrollment target
1
Study location

NCT01328704: Completed study of Anemia and Vitamin D Deficiency, sponsored by Avera McKennan Hospital & University Health Center.

NCT01328704 is a study of Anemia and Vitamin D Deficiency that has completed, run by Avera McKennan Hospital & University Health Center. The registered enrollment target is 50 participants, below the 427-participant average among 72 other Anemia trials with a reported enrollment target (88% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01328704, a study of Anemia and Vitamin D Deficiency, has completed, sponsored by Avera McKennan Hospital & University Health Center.

COMPLETED
Registry status
50 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to observe changes in iron status and vitamin D status during a 12-24 week supervised training program, specifically males and females between the ages of 30 and 50 years old.

Primary Outcome

Serum iron levels

Study Locations (1)

South Dakota

  • Avera Sports Institute - Sioux Falls

Trial Details

FieldValue
Enrollment Target 50 participants
Start Date 2012-01
Est. Completion 2013-03

What the finished NCT01328704 record still lists

NCT01328704 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 50 participants, a relatively small participant target, below the 427-participant average among 72 other Anemia trials with a reported enrollment target (88% lower).

The record links to 2 conditions, with Anemia appearing as the primary indexed condition, and to 0 interventions.

NCT01328704 reports a single indexed study location in South Dakota.

Frequently Asked Questions

What is clinical trial NCT01328704 about?

NCT01328704 is a clinical study titled "Evaluate the Change in Iron, Vitamin D, and C-Reactive Protein Level (CRP) in a 12 to 24 Week Period". The purpose of this study is to observe changes in iron status and vitamin D status during a 12-24 week supervised training program, specifically males and females between the ages of 30 and 50 years old.

What is the current status of trial NCT01328704?

This trial is currently completed. The enrollment target is 50 participants. The study started on 2012-01. Estimated completion is 2013-03.

What conditions does trial NCT01328704 study?

This clinical trial studies the following conditions: Anemia, Vitamin D Deficiency.

Who is sponsoring clinical trial NCT01328704?

This trial is sponsored by Avera McKennan Hospital & University Health Center, which has 20 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01328704 being conducted?

This trial has 1 study location across South Dakota. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Anemia

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT01328704's enrollment target sits among peer trials

50 58th of 72 higher than 14 of 72 other Anemia trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Anemia trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT01328704, the US trial registry maintained by the National Library of Medicine. NCT01328704 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.