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Effects of Pau d' Arco in Primary Dysmenorrhea

Effects of Pau d' Arco in Primary Dysmenorrhea

Recruiting
18-45 years
Female
Phase N/A
  • Simplified description (AI rewritten)
  • Technical description (Original)

This is a single arm, open-label trial evaluating safety and tolerability of 1,050 mg/day of encapsulated Tabebuia avellanedae every day for 2 months, as well as effects of the treatment on quality of life, pain intensity, and pain interference, in 12 generally healthy women aged 18-45 with PDM. Outcomes of this study include questionnaires to evaluate: safety and tolerability using standardized adverse events scales (primary); participant reported measurements of quality of life, pain intensity, and pain interference around menses collected on validated instruments (secondary); and blood concentration of PGE2 and high-sensitivity C-reactive protein (tertiary). The protocol followed the SPIRIT guidelines and fulfilled the SPIRIT checklist.

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Study details
    Primary Dysmenorrhea

NCT04245540

National University of Natural Medicine

19 February 2024

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