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Clinical Trial

Levonorgestrel Intrauterine System Effects on Hemoglobin and Serum Ferritin Among Anemic Women in Kenya

NCT: NCT05233956 · ACTIVE_NOT_RECRUITING

NCT IDNCT05233956
StatusACTIVE_NOT_RECRUITING
Start Date2023-10-23
Completion2026-12-31

Brief Summary

Women with mild/moderate anemia who are seeking contraception will be randomized to a levonorgestrel (LNG) intrauterine system (IUS) or an LNG/ethinyl estradiol (EE)/ferrous fumarate combined oral contraceptive (COC) regimen and followed prospectively for 12-18 months. Approximately 400 participants will be enrolled. The primary hypothesis that the mean change in hemoglobin in the group assigned to the LNG IUS will be superior to the COC/ferrous fumarate (control) group after 12-months of product use.

Official Source

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Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.

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