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Iron Therpay and Fatigue in Women of Reprodcutive Age

C

Central Park Medical College

Status

Completed

Conditions

Fatigue Syndrome, Chronic
Fatigue

Treatments

Drug: Placebo
Drug: Iron sucrose

Study type

Interventional

Funder types

Other

Identifiers

NCT06596161
CPMC/IRB-No/1388
CPMC (Other Identifier)

Details and patient eligibility

About

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

Enrollment

194 patients

Sex

Female

Ages

18 to 45 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

reproductive age non-anemic fatigued

Exclusion criteria

anemiac males

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

194 participants in 2 patient groups, including a placebo group

Study Group
Experimental group
Description:
Receiving Iron
Treatment:
Drug: Iron sucrose
Control Group
Placebo Comparator group
Description:
Receiving Placebo
Treatment:
Drug: Placebo

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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