A+HA Premium Oral Hyaluronic Acid Drink Functional Evaluation Trial for Delaying Joint Pain
- NCT ID
- NCT07800676
- Registry status
- Not yet recruiting
- Study type
- Interventional
- Phase
- Not applicable
- Sponsor
- Taipei Medical University
- Conditions
- Knee Pain Chronic
Overview
ClinicalTrials.gov lists this study as Not yet recruiting.
Enrollment: 60 participants (Estimated).
What is being studied
- Dietary supplement: A+HA premium oral hyaluronic acid drink
- Dietary supplement: Placebo
Who may be eligible
- Ages
- 45 Years to 80 Years
- Sex
- All
- Healthy volunteers accepted
- No
ClinicalTrials.gov lists the following eligibility criteria.
Inclusion Criteria:
1. Aged 45 to 80 years.
2. Knee osteoarthritis classified as Ahlbäck stage I or II, or Kellgren-Lawrence grade \<3.
3. A Visual Analogue Scale (VAS) pain score ≤3.
4. A Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) pain subscale score \>2 or a total WOMAC score \>12.
Exclusion Criteria:
1. Pregnant or breastfeeding women.
2. Individuals with a history of knee joint trauma or surgery.
3. A body mass index (BMI) ≥ 40 kg/m².
4. Individuals with a psychiatric disorder.
5. Individuals with severe cardiovascular disease, severe cerebrovascular disease, severe rheumatic disease, crystal deposition arthropathy, or cancer.
6. Individuals who use a wheelchair and have a Manual Muscle Testing (MMT) grade ≤3 in the lower extremities, or who require a wheelchair due to physical discomfort.
7. Use of anti-inflammatory analgesics, corticosteroids, or other medications that may affect the study outcomes within one week before the trial.
8. Receipt of intra-articular corticosteroid injections, hyaluronic acid injections, platelet-rich plasma (PRP) therapy, or nerve block treatment within one month before the trial.
9. Use of medications or consumption of foods that, in the judgment of a physician or dietitian, may affect the outcome measures.
10. Any other condition considered by the physician to make the individual unsuitable for participation in the trial.
Study locations
1 study location is listed.
Site recruitment status is not specified in the registry data for these locations.
Countries: Taiwan
Sample of listed locations
- Taipei Medical University — Taipei, Taiwan — Site recruitment status not specified in the registry data
Study details
- Start date
- September 1, 2026
- Primary completion date
- January 31, 2027
- Completion date
- February 28, 2027
- First posted
- September 2, 2026
- Collaborators
- Z-Plus Biotechnology Co., Ltd.
Source and update information
- Source
- ClinicalTrials.gov
- NCT ID
- NCT07800676
- Registry last updated
- September 2, 2026
- QualifiedStudies registry data refreshed
- October 5, 2026
- QualifiedStudies record fetched
- October 5, 2026
View NCT07800676 on ClinicalTrials.gov
Trial information can change. Confirm current study details with the study team or the registry.
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