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Effect of Hyaluronic Acid on stiffness of wrist

Evaluation of the Effect of Intra-Articular Hyaluronic Acid Injection on Postoperative Stiffness in Patients with Distal Radius Fractures Treated with Volar Plate Fixation (ORIF): A Randomized Clinical Trial

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20251202068189N1
Enrollment
60
Registered
2026-01-28
Start date
2025-12-22
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Postoperative joint stiffness, distal radius fracture, limitation of wrist range of motion. Stiffness of wrist, not elsewhere classified

Interventions

Intervention 1: Intervention group: Intervention Group (HA group): Patients will receive a single 2 mL intra-articular injection of hyaluronic acid (e.g., sodium hyaluronate 20 mg/2 mL) after wound cl

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: Adults aged 18 to 70 years Acute, closed distal radius fracture requiring ORIF with volar plate Ability and willingness to provide written informed consent and adhere to the follow-up schedule

Exclusion criteria

Exclusion criteria: Open or pathological fractures Previous surgery or trauma to the affected wrist Systemic inflammatory joint disease (e.g., rheumatoid arthritis) Known allergy to Hyaluronic Acid or its components Local or systemic infection Inability to participate in rehabilitation or follow-up Intraarticular fracture

Design outcomes

Primary

MeasureTime frame
Wrist range of motion (flexion–extension), measured using a goniometer by a blinded assessor at 12 weeks post-operation. Timepoint: Wrist flexion–extension ROM will be measured at week 6 and at week 12 after surgery. Method of measurement: Wrist joint range of motion will be measured using a standard goniometer by a trained and blinded assessor.

Secondary

MeasureTime frame
Pain intensity measured using the Visual Analogue Scale by a blinded assessor at weeks two, six, and twelve after surgery. Timepoint: Pain intensity measured at weeks two, six, and twelve after surgery. Method of measurement: Visual Analogue Scale by a blinded assessor.;Wrist functional status measured using the Quick Disabilities of the Arm, Shoulder and Hand questionnaire at weeks six and twelve after surgery. Timepoint: at weeks six and twelve after surgery. Method of measurement: the Quick Disabilities of the Arm, Shoulder and Hand questionnaire at weeks six and twelve after surgery.;Postoperative complications including persistent joint stiffness, joint swelling, and infection assessed up to week twelve after surgery. Timepoint: up to week twelve after surgery. Method of measurement: Postoperative complications including persistent joint stiffness, joint swelling, and infection will be assessed through clinical examination by the treating physician and documented using a standard clinical evaluation checklist.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactIbrahim Alkhuzaie

Tehran University of Medical Sciences

khazaei70@yahoo.com+98 915 621 0690

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 7, 2026