Skip to content

A Randomized Controlled Study on External Application of Quxie Lijie Formula Combined with Exercise Rehabilitation in Treating Cold-Dampness Obstruction Type Knee Osteoarthritis

A Randomized Controlled Study on External Application of Quxie Lijie Formula Combined with Exercise Rehabilitation in Treating Cold-Dampness Obstruction Type Knee Osteoarthritis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026000130
Enrollment
Unknown
Registered
2026-01-24
Start date
2025-12-17
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

Knee osteoarthritis

Interventions

Treatment group:External application of heated Quxie Lijie formula combined with exercise rehabilitation training
Control Group:External application of heated Quxie Lijie formula

Sponsors

Aviation General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) Aged 50-70 years, regardless of gender. (2) Meets diagnostic criteria from the 2024 Chinese Osteoarthritis Diagnosis and Treatment Guidelines. (3) Conforms to cold-dampness obstruction syndrome criteria in the 2021 Integrated Diagnosis and Treatment Guidelines for Osteoarthritis. (4) Drug washout: Patients using NSAIDs require 2-week discontinuation before enrollment; those using Adequan or corticosteroids require 1-month discontinuation. (5) Voluntary informed consent.

Exclusion criteria

Exclusion criteria: (1) Age 70 years. (2) Allergy or intolerance to experimental medications. (3) Severe primary diseases of cardiovascular, cerebrovascular, hepatic, renal or hematopoietic systems; mental disorders; epilepsy; photosensitive diseases; intracranial implants or unresolved head trauma; severe obesity (BMI=35 kg/m²); severe osteoporosis. (4) Moderate-severe osteoarthritis (K&L grade III-IV). (5) Previous knee replacement, ligament reconstruction or arthroscopic surgery; recent (within 6 months) lower limb fracture or surgery. (6) Inability to complete assessments. (7) Non-KOA related balance disorders (e.g., vestibular dysfunction, spinal lesions). (8) Refusal to sign informed consent.

Design outcomes

Secondary

MeasureTime frame
Lyshom Knee Rsting System;TCM Symptom Efficacy Evaluation;Isokinetic Dynamometry;Balance Function Assessment;Cerebral Cortex Activation Pattern Assessment;

Primary

MeasureTime frame
Arthritis Pain Assessment (VAS);Western Ontario and McMaster Osteoarthritis Index;

Countries

China

Contacts

Public ContactWang Wanru

Aviation General Hospital

764482182@qq.com18611412318

Outcome results

None listed

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