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Study on efficacy and safety of high molecular weight hyaluronic acid "Hylan G-F 20" for patients with osteoarthritis of the hip

Study on efficacy and safety of high molecular weight hyaluronic acid "Hylan G-F 20" for patients with osteoarthritis of the hip - Efficacy and safety of Hylan G-F 20 injection for hip osteoarthritis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000018000
Enrollment
30
Registered
2015-06-23
Start date
2012-04-27
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Osteoarthritis of the hip

Interventions

Intraarticular injection of Hylan G-F 20 for osteoarthritis of the hip

Sponsors

Department of Orthopaedic Surgery, Tokyo Medical and Dental University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients meeting all following (1)-(4) at registration are adopted. (1) Patients diagnosed OA of hip joint. (2) Outpatients who can walk. (3) Patients aged 20-84 years. (4) Patients who submitted the consent of this study before the registration by understanding the method.

Exclusion criteria

Exclusion criteria: Exclusion criteria of the patients are as follows. (1) Patients lacking ability to agree or ability to express agreement for participation appropriately in this study. (2) Pregnancy or its possibility. (3) Patients suckling child. (4) Patients with hypersensitivity for the ingredient of this medicine, hyaluronic acid, avian protein, feather, or egg. (5) Patients with stagnation of venous blood or lymph fluid in lower limbs on injection side. (6) Patients with a serious liver damage or its medical history. (7) Patients with skin disease or with infection on the injection part. (8) Patients with serious complications (heart disorder, renal disease, a malignant tumor, or compromised host such as immunodeficiency). (9) Patients judged inadequate by the attending doctor.

Design outcomes

Primary

MeasureTime frame
Physical findings and patient-based subjective assessment right after, 4, 8, and 12 weeks after intra-articular injection of hyaluronic acid

Secondary

MeasureTime frame
Incidence of adverse events

Countries

Japan

Contacts

Public ContactGaku Koyano

Tokyo Medical and Dental University Department of Orthopaedic Surgery

gaku@mtb.biglobe.ne.jp03-3813-6111

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026