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Evaluation of Flexofytol® PLUS in Hand Joint Chronic Dyscomfort.

NCT05089318 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 239

Last updated 2023-04-12

No results posted yet for this study

Summary

The purpose of this study is to evaluate the effect of curcuminoids and Boswellia serrata extracts combination (Flexofytol PLUS) in support to standard treatments during a 12-weeks period on hand pain on people with chronic hand joint discomfort.

Conditions

  • Hand Joint Discomfort

Interventions

DIETARY_SUPPLEMENT

Flexofytol PLUS

2 tablets in the morning and in the evening for minimum 6 weeks.

Sponsors & Collaborators

  • Tilman S.A.

    lead INDUSTRY

Principal Investigators

  • Yvan Dierckxsens · Tilman S.A.

Eligibility

Min Age
45 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-09-01
Primary Completion
2021-09-01
Completion
2021-09-01

Countries

  • Belgium

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05089318 on ClinicalTrials.gov