Iron Therpay and Fatigue in Women of Reprodcutive Age

Central Park Medical College194 enrolled

Overview

For the assessment of anemia and then assessment of fatigue levels in non-anemic women followed by assessment of iron levels and intervention of iron and placebo

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

DOUBLE

Enrollment

194

Conditions

Fatigue Syndrome, Chronic Fatigue

Interventions

Iron sucroseDRUG

Receving iron

PlaceboDRUG

Placebo

Eligibility

Sex: FEMALEMin age: 18 YearsMax age: 45 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: reproductive age non-anemic fatigued Exclusion Criteria: anemiac males

Locations (1)

Central Park Teaching Hospital

Lahore, Punjab Province, Pakistan

Outcomes

Primary Outcomes

Fatigue Score improvemnt

improvement in fatigue levels

Time frame: 60 days

Data from ClinicalTrials.gov

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