# Effects of Oral Iron on Postoperative Fatigue Upon Coronary Artery Bypass Graft Patients

> **NCT01912261** · PHASE3 · TERMINATED · sponsor: **Nova Scotia Health Authority** · enrollment: 121 (actual)

## Conditions studied

- Fatigue

## Interventions

- **DRUG:** Placebo
- **DRUG:** Polysaccharide iron complex

## Key facts

- **NCT ID:** NCT01912261
- **Lead sponsor:** Nova Scotia Health Authority
- **Sponsor class:** OTHER
- **Phase:** PHASE3
- **Study type:** INTERVENTIONAL
- **Status:** TERMINATED
- **Start date:** 2014-12-16
- **Primary completion:** 2018-02-21
- **Final completion:** 2019-02
- **Target enrollment:** 121 (ACTUAL)
- **Why stopped:** The study was stopped due to time constraints and resources
- **Last updated:** 2019-07-26

## Collaborators

- [object Object]
- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT01912261

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT01912261, "Effects of Oral Iron on Postoperative Fatigue Upon Coronary Artery Bypass Graft Patients". Retrieved via AI Analytics 2026-06-08 from https://api.ai-analytics.org/clinical/NCT01912261. Licensed CC0.

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