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Clinical Trial Summary

This is a prospective randomized-controlled trial looking at the safety and acceptability of using Chinese herbal medicine in patients with primary dysmenorrhea. The research team hopes to enroll 100 patients, 50 of whom will be randomized to receive the herbal tincture and 50 who will receive a placebo tincture. Patients will be enrolled and using the assigned tincture for twelve weeks. The research team will assess safety as a primary outcome by the presence or absence of adverse events related to study protocol during the period of participation.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06187376
Study type Interventional
Source Icahn School of Medicine at Mount Sinai
Contact Nicola Tavella, MPH
Phone (212) 241-3888
Email nicola.tavella@mssm.edu
Status Not yet recruiting
Phase Phase 2
Start date July 2024
Completion date July 2025

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