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Oral Iron Substitution for Orthopedic Surgery

NCT02973074 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2018-08-09

No results posted yet for this study

Summary

The aim of this pilot study is to investigate an 4 weeks period of oral iron substitution in the course of Patient Blood Management in preparation for orthopedic surgery.

Conditions

Interventions

DIETARY_SUPPLEMENT

OLEOvital

2sachets with 30mg iron per day for a 4 weeks period

Sponsors & Collaborators

  • Kepler University Hospital

    lead OTHER

Principal Investigators

  • Jens Meier, Prof. Dr. · Kepler University Hospital Linz, Clinic for Anesthesiology and intensive care medicine

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
55 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-11-25
Primary Completion
2017-11-01
Completion
2017-11-01

Countries

  • Austria

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02973074 on ClinicalTrials.gov