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CompletedNCT07241442Updated Feb 27, 2026

Cross-linked Hyaluronic Acid in Knee Osteoarthritis

An observational study in Knee Osteoarthritis (Knee OA), sponsored by Istanbul Medipol University Hospital. Completed at 1 site in Turkey (Türkiye). Open to participants aged 50 Years to 70 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-02-27.

Sponsored by Istanbul Medipol University Hospital · Observational

Study type
Observational
Model
Case-control
Time perspective
Retrospective
Enrollment
88
Ages
50 Years to 70 Years
Sex
All
01

Study summary

Knee Osteoarthritis (Knee OA) leads to pain and loss of function, especially in recreational athletes. While hyaluronic acid (HA) injections are a common part of conservative treatment, comparative data on the efficacy of straight-chain (ST-HA) versus cross-linked (CL-HA) formulations remain limited. Therefore, the aim of this study was to compare the 6-month efficacy of a single dose of CL-HA versus two doses of ST-HA regarding pain, stiffness, and joint function in recreational athletes aged 50-70 with Kellgren-Lawrence grade 2-3 Knee OA refractory to pharmacological treatment.

Read the detailed description

This retrospective observational study included 88 recreational athletes (CL-HA: n=44, ST-HA: n=44). All participants received either a single dose of CL-HA or two doses of ST-HA administered 4 weeks apart. Patients were comparatively evaluated pre-treatment and at 1, 3, and 6 months post-treatment using the WOMAC (Western Ontario and McMaster Universities Osteoarthritis Index) and VAS scores.

02

Conditions studied

  • Knee Osteoarthritis (Knee OA)

Keywords

  • Knee Osteoarthritis, Cross-linked Hyaluronic Acid, Recreational Athletes, Intra-articular Injection, WOMAC
03

In context

Osteoarthritis, Knee

3,302 studies on the registry are indexed under Osteoarthritis, Knee; 608 are open to participants now.

This study's enrollment of 88 is below the median of 100 across 472 observational studies indexed under Osteoarthritis, Knee.

Browse Osteoarthritis, Knee studies →

Lead sponsor

Istanbul Medipol University Hospital is the lead sponsor of 350 studies on the registry; 58 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
50 Years to 70 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

This retrospective observational study was conducted in a multicenter manner and included recreational athletes aged between 50 and 70 years who applied to Medipol Esenler Hospital and Republic of Turkey Ministry of Health Erenköy Physical Therapy and Rehabilitation Hospital due to knee pain and were diagnosed with gonarthrosis between January 2021 and December 2024.

Eligibility criteria

Inclusion Criteria: Inclusion criteria: Recreational athletes aged 50-70 years; participants must not have received any injections or undergone physical therapy or rehabilitation in the last 3 months; and symptomatic cases of Kellgren-Lawrence stage 2-3 knee osteoarthritis and failure of pharmacological treatment.

Exclusion Criteria: Inflammatory disease, active rheumatic disease, malignancy, bleeding diathesis, peripheral neuropathy, BMI >30, grade 4 gonarthrosis, regular NSAID use, previous knee surgery, local infection at the procedure site, corticosteroid injection at the procedure site within the last 3 months, systemic corticosteroid use within the last 2 weeks, immunosuppressant use or immunodeficiency within the last 6 weeks, and any local or systemic osteoarthritis-related treatments (therapeutic exercises, physical therapy, other injections, NSAIDs, etc.) within the last 6 months.

05

Study design

Observational model
Case-control
Time perspective
Retrospective
Enrollment
88 participants (actual)
Patient registry
No

Interventions

  • DrugStraight-bonded hyaluronic acid

    Straight-bonded HA injection was applied in 2 doses, 4 weeks apart.

  • Drugcross-linked hyaluronic acid

    Cross-linked HA was applied as a single dose to the knee via the anterolateral approach.

06

What researchers measure

Primary outcomes

  1. Patients were comparatively evaluated pre-treatment and at 1, 3, and 6 months post-treatment using the WOMAC (Western Ontario and McMaster Universities Osteoarthritis Index) score.

    Minimal value is 0, while maximum value is 96.

    Time frame: Patients were comparatively evaluated pre-treatment and at 1, 3, and 6 months post-treatment

Secondary outcomes

  1. Patients were comparatively evaluated pre-treatment and at 1, 3, and 6 months post-treatment using the VAS score.

    Minimal value is 0, while maximum value is 10.

    Time frame: Patients were comparatively evaluated pre-treatment and at 1, 3, and 6 months post-treatment

07

Study locations

1 site
  • Istanbul Medipol University
    Istanbul, Turkey (Türkiye)
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References and documents

Individual participant data

Plan to share: Yes — After publication in a journal, I will share all IPD that underlie results in a publication

Supporting information: Study protocol, Sap

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 27, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07241442
Lead sponsor
Istanbul Medipol University Hospital
Responsible party
Seyda Ersahan, DDS, PhD (Assoc.Prof., Istanbul Medipol University Hospital) — Principal investigator
First posted
Nov 21, 2025
Start date
Jan 2, 2021
Primary completion
Dec 31, 2024
Completion
May 31, 2025
Last update
Feb 27, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Feb 2026. You cannot join it, but the record below documents what was studied.

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