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The Effectiveness of Different Doses of Hyaluronic Acid Injections in Knee Osteoarthritis.

Primary Purpose

Knee Osteoarthritis

Status
Completed
Phase
Not Applicable
Locations
Turkey
Study Type
Interventional
Intervention
Intra-articular 20 mg, 1.0% Hyaluronic Acid Injection
Intra-articular 32 mg, 1.6% Hyaluronic Acid Injection
Intra-articular 48 mg, 2.0% Hyaluronic Acid Injection
Sponsored by
Istanbul University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Knee Osteoarthritis focused on measuring Knee Osteoarthritis, Linear Hyaluronic Acid

Eligibility Criteria

45 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Unilateral or bilateral symptomatic knee pain for at least three months
  • Presence of Kellgren-Lawrence stage 2-3 osteoarthritis on current anterior-posterior knee radiographs
  • Functional ambulation scale stage 4-5
  • Being able to attend injection and control examinations

Exclusion Criteria:

  • Intra-articular knee injection within the last six months
  • History of severe trauma to the knee within the past six months
  • Concomitant severe meniscus or ligament injury, surgery applied to the knee area
  • Presence of severe effusion, inflammatory joint disease, infection, hematological and oncological disease in the knee.
  • Having a bleeding disorder and / or using warfarin
  • Kellgren-Lawrence stage 1 or stage 4 osteoarthritis on current anterior-posterior knee radiographs
  • Presence of cardiac or systemic disease that may affect exercise
  • The presence of neurological disease and psychiatric disease such as Parkinson's disease, stroke history that may affect balance
  • Body Mass Index ≥35 kg / m²
  • Allergy to hyaluranic acid products

Sites / Locations

  • Istanbul University Istanbul Faculty of Medicine, Department of Physical Medicine and Rehabilitation

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

Active Comparator

Arm Label

20 mg, 1.0% hyaluronic acid injection groups

32 mg, 1.6% hyaluronic acid injection groups

48 mg, 2.0% hyaluronic acid injection groups

Arm Description

In the first group, 2 ml linearly linked 20 mg 1.0% hyaluronic acid injection in 5 sessions will be applied.

In the second group, 2 ml linearly linked 32 mg 1.6% hyaluronic acid injection in 3 sessions will be applied.

In the third group 2.4 ml linearly linked 48 mg 2.0% hyaluronic acid injection in a single sessions will be applied.

Outcomes

Primary Outcome Measures

Change from baseline activity pain score at 1-months, 3-months and 6-months
Visual Analogue Scale-Activity pain (0-10 point). Higher scores mean a worse outcome

Secondary Outcome Measures

Change from baseline rest pain score at 1-months, 3-months and 6-months
Visual Analogue Scale-Rest pain (0-10 point). Higher scores mean a worse outcome
Change from baseline night pain score at 1-months, 3-months and 6-months
Visual Analogue Scale-Night pain (0-10 point). Higher scores mean a worse outcome
Change from baseline pain, stiffness and physical function at 1-months, 3-months and 6-months
Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) measures knee pain, stiffness, and physical function. The scores for each subscale are summed up, with a possible score range of 0-20 for Pain, 0-8 for Stiffness, and 0-68 for Physical Function. The sum of the scores for the three subscales gives a total WOMAC score. High scores are associated with more pain, stiffness, and poor function, while low scores indicate well-being.
Change from baseline functional balance at 1-months, 3-months and 6-months
The Timed Up and Go test requires the person to stand up from a standard chair in which they are sitting, walk 3 m at a comfortable speed to the marked place on the floor, turn around, walk backwards to the starting point and return to the sitting position in the chair. The time taken for the person to complete the test is measured in seconds. The timing of the test is related to the function.

Full Information

First Posted
March 3, 2021
Last Updated
October 16, 2022
Sponsor
Istanbul University
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1. Study Identification

Unique Protocol Identification Number
NCT04786613
Brief Title
The Effectiveness of Different Doses of Hyaluronic Acid Injections in Knee Osteoarthritis.
Official Title
The Efficacy and Safety of Intra-articular Injections of 48 mg, 32 mg and 20 mg Linear Hyaluronic Acid in Patients With Knee Osteoarthritis: A Multicenter Randomized Single-Blind Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
October 2022
Overall Recruitment Status
Completed
Study Start Date
March 10, 2021 (Actual)
Primary Completion Date
October 7, 2021 (Actual)
Study Completion Date
November 7, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Istanbul University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The aim of this prospective, randomized, controlled multi-centre study is to compare the effectiveness and safety of three and five injections of standard linear hyaluronic acid (HA) versus single HA injection in terms of pain intensity and functional status in patients with knee osteoarthritis.
Detailed Description
Osteoarthritis (OA) is the most common form of chronic joint disease. A treatment option for patients diagnosed with knee osteoarthritis is intra-articular hyaluronic acid therapy. In this prospective, randomized controlled, single blind, interventional study, a total of 90 patients with stage 2-3 knee osteoarthritis according to the kellgren lawrence classification who meet the eligibility criteria will be enrolled in the study. Eligible participants will be randomly assigned to one of the three groups using computer-generated random numbers. In the first group, 2 ml linearly linked 20 mg 1.0% hyaluronic acid injection in 5 sessions, in the second group 2 ml linearly linked 32 mg 1.6% hyaluronic acid injection in 3 sessions and in the third group 2.4 ml linearly linked 48 mg 2.0% hyaluronic acid injection in a single sessions will be applied. Participants are going to evaluate before injection, at the 1-month follow-up, at the 3-month follow-up and 6-month follow-up using the visual analog scale (VAS) scores for pain during activity, at rest, and at night, with the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) change in pain, stiffness and physical function score, the change in the Timed Up and Go Test (TUG) time and the change in the patient's daily activities with the numerical global patient assessment scale.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Knee Osteoarthritis
Keywords
Knee Osteoarthritis, Linear Hyaluronic Acid

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
InvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
100 (Actual)

8. Arms, Groups, and Interventions

Arm Title
20 mg, 1.0% hyaluronic acid injection groups
Arm Type
Active Comparator
Arm Description
In the first group, 2 ml linearly linked 20 mg 1.0% hyaluronic acid injection in 5 sessions will be applied.
Arm Title
32 mg, 1.6% hyaluronic acid injection groups
Arm Type
Active Comparator
Arm Description
In the second group, 2 ml linearly linked 32 mg 1.6% hyaluronic acid injection in 3 sessions will be applied.
Arm Title
48 mg, 2.0% hyaluronic acid injection groups
Arm Type
Active Comparator
Arm Description
In the third group 2.4 ml linearly linked 48 mg 2.0% hyaluronic acid injection in a single sessions will be applied.
Intervention Type
Other
Intervention Name(s)
Intra-articular 20 mg, 1.0% Hyaluronic Acid Injection
Intervention Description
Intra-articular 2 ml linearly linked 20 mg 1.0% hyaluronic acid injection in 5 sessions will be applied. As a home exercise program, hamstring and quadriceps stretching, quadriceps isometric strengthening, short arc terminal extension exercises will be given at least three days a week with 3 sets of 10 repetitions.
Intervention Type
Other
Intervention Name(s)
Intra-articular 32 mg, 1.6% Hyaluronic Acid Injection
Intervention Description
Intra-articular 2 ml linearly linked 32 mg 1.6% hyaluronic acid injection in 3 sessions will be applied. As a home exercise program, hamstring and quadriceps stretching, quadriceps isometric strengthening, short arc terminal extension exercises will be given at least three days a week with 3 sets of 10 repetitions.
Intervention Type
Other
Intervention Name(s)
Intra-articular 48 mg, 2.0% Hyaluronic Acid Injection
Intervention Description
Intra-articular 2,4 ml linearly linked 48 mg 2.0% hyaluronic acid injection in single session will be applied. As a home exercise program, hamstring and quadriceps stretching, quadriceps isometric strengthening, short arc terminal extension exercises will be given at least three days a week with 3 sets of 10 repetitions.
Primary Outcome Measure Information:
Title
Change from baseline activity pain score at 1-months, 3-months and 6-months
Description
Visual Analogue Scale-Activity pain (0-10 point). Higher scores mean a worse outcome
Time Frame
Baseline, 1-month, 3-month, 6-month
Secondary Outcome Measure Information:
Title
Change from baseline rest pain score at 1-months, 3-months and 6-months
Description
Visual Analogue Scale-Rest pain (0-10 point). Higher scores mean a worse outcome
Time Frame
Baseline, 1-month, 3-month, 6-month
Title
Change from baseline night pain score at 1-months, 3-months and 6-months
Description
Visual Analogue Scale-Night pain (0-10 point). Higher scores mean a worse outcome
Time Frame
Baseline, 1-month, 3-month, 6-month
Title
Change from baseline pain, stiffness and physical function at 1-months, 3-months and 6-months
Description
Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) measures knee pain, stiffness, and physical function. The scores for each subscale are summed up, with a possible score range of 0-20 for Pain, 0-8 for Stiffness, and 0-68 for Physical Function. The sum of the scores for the three subscales gives a total WOMAC score. High scores are associated with more pain, stiffness, and poor function, while low scores indicate well-being.
Time Frame
Baseline, 1-month, 3-month, 6-month
Title
Change from baseline functional balance at 1-months, 3-months and 6-months
Description
The Timed Up and Go test requires the person to stand up from a standard chair in which they are sitting, walk 3 m at a comfortable speed to the marked place on the floor, turn around, walk backwards to the starting point and return to the sitting position in the chair. The time taken for the person to complete the test is measured in seconds. The timing of the test is related to the function.
Time Frame
Baseline, 1-month, 3-month, 6-month

10. Eligibility

Sex
All
Minimum Age & Unit of Time
45 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Unilateral or bilateral symptomatic knee pain for at least three months Presence of Kellgren-Lawrence stage 2-3 osteoarthritis on current anterior-posterior knee radiographs Functional ambulation scale stage 4-5 Being able to attend injection and control examinations Exclusion Criteria: Intra-articular knee injection within the last six months History of severe trauma to the knee within the past six months Concomitant severe meniscus or ligament injury, surgery applied to the knee area Presence of severe effusion, inflammatory joint disease, infection, hematological and oncological disease in the knee. Having a bleeding disorder and / or using warfarin Kellgren-Lawrence stage 1 or stage 4 osteoarthritis on current anterior-posterior knee radiographs Presence of cardiac or systemic disease that may affect exercise The presence of neurological disease and psychiatric disease such as Parkinson's disease, stroke history that may affect balance Body Mass Index ≥35 kg / m² Allergy to hyaluranic acid products
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Demirhan Diracoglu, Prof.
Organizational Affiliation
Istanbul University Istanbul Faculty of Medicine, Department of Physical Medicine and Rehabilitation
Official's Role
Principal Investigator
Facility Information:
Facility Name
Istanbul University Istanbul Faculty of Medicine, Department of Physical Medicine and Rehabilitation
City
Istanbul
State/Province
Fatih
ZIP/Postal Code
34034
Country
Turkey

12. IPD Sharing Statement

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The Effectiveness of Different Doses of Hyaluronic Acid Injections in Knee Osteoarthritis.

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