Clinical Trials Logo

Clinical Trial Summary

The purpose of this study is to examine whether daily supplementation of resveratrol would improve bone health in postmenopausal women.


Clinical Trial Description

34 women will be randomly assigned to two groups: 1) the placebo group and 2) the resveratrol group. The resveratrol group will receive 500 mg resveratrol daily for 24 weeks, and placebo group will receive placebo pills. Both groups will receive 500 mg calcium plus 400 IU vitamin D daily. Blood and urinary biomarkers of bone metabolism will be assessed at baseline and after 12 and 24 weeks intervention. Bone mineral density will be assessed using dual-energy X-ray absorptiometry at baseline and after 24 weeks. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06250283
Study type Interventional
Source University of Delaware
Contact Sheau Ching Chai, PhD, RD
Phone 302-831-7345
Email scchai@udel.edu
Status Recruiting
Phase N/A
Start date February 2, 2024
Completion date December 31, 2024

See also
  Status Clinical Trial Phase
Completed NCT00980174 - Study to Compare the Efficacy and Safety of DenosumAb Versus Placebo in Males With Osteoporosis Phase 3
Completed NCT00887965 - A Transiliac Crest Bone Histology and Histomorphometry Study in Postmenopausal Women With Low Bone Mass or Osteoporosis Previously Treated With Denosumab Phase 2
Completed NCT00890981 - A High-resolution Peripheral Quantitative Computed Tomography Study in Postmenopausal Women Previously Treated With Denosumab Phase 3
Active, not recruiting NCT03227458 - DHEA Augmentation of Musculoskeletal Adaptations to Exercise in Older Women N/A