U.S., March 28 -- ClinicalTrials.gov registry received information related to the study (NCT06899243) titled 'Efficacy of CL22205 on Bone Mineral Density and Menopausal Symptoms' on March 01.
Brief Summary: The purpose of this study is to evaluate the effect of CL22205 on bone mineral density and menopausal symptoms in women.
Study Start Date: March 25
Study Type: INTERVENTIONAL
Condition:
Menopausal Symptoms
Intervention:
DIETARY_SUPPLEMENT: CL22205
200 mg, Route : Oral, One capsule a day after breakfast for 360 days
OTHER: Placebo
Route : Oral, One capsule a day after breakfast for 360 days
Recruitment Status: NOT_YET_RECRUITING
Sponsor: Eetho Brands, Inc
Disclaimer: Curated by HT Syndication....