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OpenTrials
Completed

NCT Number: NCT06596161

Iron Therpay and Fatigue in Women of Reprodcutive Age

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

Completed

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Key information

Age range

18 year–45 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Central Park Teaching Hospital

Lahore, Punjab Province, Pakistan

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

reproductive age non-anemic fatigued

Exclusion criteria

anemiac males

Treatment and study plan

Iron sucrose

Drug

Receving iron

Placebo

Drug

Placebo

Primary outcomes

  1. Fatigue Score improvemnt

    Time frame: 60 days

    improvement in fatigue levels

Sponsors and collaborators

Lead sponsor

Central Park Medical College

Other

Registry information

Official study title

Effect or Iron Therapy on Fatigue Symptoms in Non-anemic Iron Deficient Women of Reproductive Age

Important dates

Study start
2023
Primary completion
2024
Study completion
2024
First posted
Sep 19, 2024
Registry last updated
Sep 19, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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