None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Adults of either gender with primary tibiofemoral knee osteoarthritis fulfilling ACR clinical and radiographic criteria, radiographic Kellgren Lawrence grade II or III, and body mass index less than 40, who are willing to provide written informed consent.
Exclusion criteria
Exclusion criteria: History of bleeding disorders; any acute injury or recent surgery within the past three months; use of anti-inflammatory drugs for more than seven days in the past four weeks or within five days before starting the trial; current use of corticosteroids or immunosuppressive drugs; presence of any acute co-existing illness; prior hyaluronic acid injection or unwillingness to receive hyaluronic acid; any overlying skin infection; venous or lymphatic stasis.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Timepoint: | — |
Secondary
| Measure | Time frame |
|---|---|
| NILTimepoint: NIL | — |
Countries
India
Contacts
Vardhman Mahavir Medical College and Safdarjung hospital