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A Clinical Study on Sodium Hyaluronate Combined with Zhengqing Fengtongning in Treatment of Frozen Shoulder

A Clinical Study on Sodium Hyaluronate Combined with Zhengqing Fengtongning in Treatment of Frozen Shoulder

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300074986
Enrollment
Unknown
Registered
2023-08-22
Start date
2023-09-01
Completion date
Unknown
Last updated
2023-08-28

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

Conditions

frozen shoulder

Interventions

Zhengqing Fengtongning group:ZF group was marked the affected side acupoints (Jianqian, Jianyu, Jianliao, Jianjing, Quchi) with a marker. 5mL syringe (22G needle) extracted ZF injection (Hunan Zhengqi
Sodium Hyaluronate group:SH group was marked the puncture point of shoulder joint cavity with a marker. Disinfected in the same way, the 21G needle was inserted into shoulder joint cavity vertically f
combined use group:ZF + SH group was treated with the operation of ZF group firstly, and then the SH group. Once a week, 5 times in total.

Sponsors

Affiliated Hospital of Hunan Academy of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Those who met the diagnostic criteria for periarthritis of shoulder in the 2019 edition of the Clinical Guidelines for Diagnosis and Treatment in Traditional Chinese Medicine Orthopedics and Traumatology or the adhesive capsulitis in the 11 th revision of the International Classification of Diseases. (2) No treatment (including medication and other treatment modalities) within the last 1 month that may affect the efficacy of this study. (3) Those who were generally in good condition with stable vital signs. (4) Those who agreed to participate in this study and signed the informed consent form.

Exclusion criteria

Exclusion criteria: (1) Those who refused to participate in this study. (2) Those who had a history of trauma to the shoulder joint or a combination of other shoulder joint peripheral lesions. (3) Treatment (including medication and other treatment modalities) that may affect the efficacy of this study had been carried out in recent 1 month. (4) Allergic to the drugs used in this study. (5) Those who were contraindicated to the use of drugs in this study.

Design outcomes

Primary

MeasureTime frame
visual analogue scale;Constant-Murley Shoulder Rating Scale;Pittsburgh sleep quality index;

Countries

China

Contacts

Public ContactGuanbao WU

Affiliated Hospital of Hunan Academy of Traditional Chinese Medicine

yhywgb@126.com+86 138 7591 7858

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026