Evaluation of the Effect of Pro Resolve® Sports on Treatment of Patients With Symptomatic Knee Osteoarthritis

NACompletedINTERVENTIONAL
Enrollment

100

Participants

Timeline

Start Date

May 30, 2018

Primary Completion Date

October 14, 2021

Study Completion Date

October 14, 2021

Conditions
Knee Osteoarthritis
Interventions
DIETARY_SUPPLEMENT

SMP group

Participants were instructed to take two 500 mg softgels of LIPINOVA(SPM group) after breakfast and two after dinner during the first 6 weeks of the study. During the next 6 weeks, participants were instructed to take one softgel after breakfast and one after dinner. Thus, the treatment period was 12 weeks

DIETARY_SUPPLEMENT

Placebo group

Participants were instructed to take two 500 mg softgels of olive oil placebo after breakfast and two after dinner during the first 6 weeks of the study. During the next 6 weeks, participants were instructed to take one softgel after breakfast and one after dinner. Thus, the treatment period was 12 weeks

Trial Locations (5)

Unknown

Clínica Segura, Las Rozas de Madrid

Clínica Dr. Rodas, Avilés

Medical Services Ath, Club Bilbao, Bilbao

Instituto Poal de Reumatología, Barcelona

Medical Services F.C. Barcelona, Barcelona

All Listed Sponsors
collaborator

OAFI Foundation (Osteoarthritis Foundation International)

UNKNOWN

lead

Solutex GC S.L.

INDUSTRY

NCT05633849 - Evaluation of the Effect of Pro Resolve® Sports on Treatment of Patients With Symptomatic Knee Osteoarthritis | Biotech Hunter | Biotech Hunter