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Clinical Trial Summary

Interventional, randomised, prospective, monocentric study


Clinical Trial Description

Interventional, randomised, prospective, monocentric study Primary objective : Demonstrate the interest of the homeopathic Protocol to reduce the onset or aggravation of joint pain as a result of the taking of AI compared to conventional care Secondary objective : Compare between the two treatment groups: - Evolution of joint pain - Evolution of joint stiffness-rate of onset of pain and joint stiffness-delay in onset or aggravation of pain-evolution of the number of painful locations-evolution of the impact of pain on the quality of the sleep-consumption of permitted concomitant treatments (analgesics) - Evolution of symptoms of hormonal deprivation-adherence to AI treatment - Tolerance to AI - Change seen by patients - Stop rate and switch of AI-rate of recurrence of breast cancer Describe in patients receiving homeopathic treatment: - Adherence to homeopathic treatment - Tolerance to homeopathic treatment - Group A: Group of patients receiving conventional treatment (drug analgesic class 1) for joint pain + homeopathic treatment - Group B: Group of patients receiving conventional treatment (drug analgesic class 1) for joint pain Schedule : - Inclusions start at: 01/09/2018 - End date of inclusions: 01/09/2021 - End date of follow-up: 23/03/2022 - Study report: 23/03/2023 ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04408560
Study type Interventional
Source Institut Jean-Godinot
Contact
Status Completed
Phase N/A
Start date September 13, 2018
Completion date March 23, 2022

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