Iron Therpay and Fatigue in Women of Reprodcutive Age

Not Applicable

Completed

• Conditions: Fatigue Syndrome, Chronic; Fatigue
• Interventions: Drug: Iron sucrose; Drug: Placebo

• Registration Number: NCT06596161
• Lead Sponsor: Central Park Medical College

Brief Summary

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

Detailed Description

Not available

Study Timeline

• Study Start: 2023-02-25
• Primary Completion: 2024-02-20
• Study Completion: 2024-03-02
• Status Verified: 2024-09
• Study First Submitted: 2024-09-11
• Study First Submitted QC: 2024-09-11
• Last Update Submitted: 2024-09-11
• Study First Posted: 2024-09-19
• Last Update Posted: 2024-09-19

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Female
• Target Recruitment: 194

Inclusion Criteria

reproductive age non-anemic fatigued

Exclusion Criteria

anemiac males

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Study Group	Iron sucrose	Receiving Iron
Control Group	Placebo	Receiving Placebo

Primary Outcome Measures

Name	Time	Method
Fatigue Score improvemnt	60 days	improvement in fatigue levels

Trial Locations

Locations (1)

Central Park Teaching Hospital; 🇵🇰 Lahore, Punjab, Pakistan