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Combination of Platelets Rich Plasma and Hyaluronic is an Effective Tool for Treatment of Knee Osteoarthritis

U

University of Karachi

Status

Completed

Conditions

Knee Osteoarthristis

Treatments

Drug: Hyaluronic Acid (HA)
Drug: Hyaluronic Acid (HA) and Platelet rich plasma
Drug: Platelet Rich Plasma

Study type

Interventional

Funder types

Other

Identifiers

NCT07089446
SCH-IRB-2022-05

Details and patient eligibility

About

The purpose of the study is to determine the effects of HA, PRP and the combination of HA and PRP in reducing pain and improving functional disability in patients with knee osteoarthritis.

Full description

To determine the effects of combination of platelet rich plasma (PRP) and hyaluronic acid and the PRP or HA alone in reducing pain and increasing range of motion among individuals with knee osteoarthritis.

Enrollment

60 patients

Sex

All

Ages

40 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • grade II-III according to the Kellgren-Lawrence classification),
  • pain or functional limitations in patients' activity of daily living before the treatment,
  • age between 40 and 70 years of age, and the absence of clinical or imaging signs of articular instability.

Exclusion criteria

  • includes known hypersensitivity to hyaluronic acid,
  • pregnancy and lactation, a BMI greater than 40 kg/m2,
  • chronic administration of anticoagulant drugs or a history of coagulopathies,
  • neoplastic lesions, and knee or kidney failures

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

60 participants in 3 patient groups

Group A
Experimental group
Description:
Hyaluronic acid
Treatment:
Drug: Hyaluronic Acid (HA)
Group B
Active Comparator group
Description:
platelet rich plasma
Treatment:
Drug: Platelet Rich Plasma
Group C
Other group
Description:
Hyaluronic acid and platelet rich plasma
Treatment:
Drug: Hyaluronic Acid (HA) and Platelet rich plasma

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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