Clinical Trials Directory

Trials / Completed

CompletedNCT06665516

Frequency and Impact of Iron Deficiency in Pain Clinic Patients

Status
Completed
Phase
Study type
Observational
Enrollment
81 (actual)
Sponsor
McMaster University · Academic / Other
Sex
Female
Age
18 Years – 49 Years
Healthy volunteers
Not accepted

Summary

The goal of this study is to measure the proportion of patients who have iron deficiency and if iron deficiency is treated what is the outcome. Participants will fill out a questionnaire to assess positive impact of iron supplementation treatment to assess whether they are at potential risk of iron deficiency

Detailed description

The study is an observational clinical audit, with an unblinded clinical intervention. Iron deficiency and some chronic pain syndromes like fibromyalgia are more common in women of reproductive age. Iron deficiency can present with symptoms that are similar to those of fibromyalgia, but once recognized, iron deficiency is typically easily treated. The investigators intend to poll patients at the DeGroote Pain Clinic based on information from studies conducted in Australia and Great Britain. The investigators will determine who is at risk for iron deficiency based upon symptoms such as heavy periods, history of pregnancy, blood donation, diet, and any previous iron deficiency. The investigators will then confirm the results with lab testing, and provide treatment if necessary. The goal is to find out the percentage of women with chronic pain who also have iron deficiency, and assess the effect of treating iron deficiency on their pain symptoms.

Conditions

Timeline

Start date
2025-03-19
Primary completion
2025-06-09
Completion
2025-06-09
First posted
2024-10-30
Last updated
2025-12-09

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT06665516. Inclusion in this directory is not an endorsement.