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Clinical efficacy of Qi Huang Needle therapy in the treatment of mid-term postoperative pain after rotator cuff repair

Clinical efficacy of Qi Huang Needle therapy in the treatment of mid-term postoperative pain after rotator cuff repair

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300069347
Enrollment
Unknown
Registered
2023-03-14
Start date
2023-03-15
Completion date
Unknown
Last updated
2023-05-29

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

Conditions

postoperative pain after rotator cuff repair

Interventions

Huang Needle therapy + Basic Treatment group:N/A
Basic Treatment group:N/A

Sponsors

The First Affiliated Hospital of Guangzhou University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Aged 30-70 years; 2. Arthroscopic rotator cuff repair performed by the same chief physician of the Department of Sports Medicine with an intraoperative measurement of 10 mm - 50 mm width before and after rotator cuff tear; 3. MR of the affected shoulder after 6 weeks of routine postoperative fixation in an abductor brace suggests good continuity after rotator cuff repair, but still has pain in the shoulder on the operated side (resting pain, active pain, nocturnal pain) and either VAS pain score >= 30 mm; 4. Those who are willing and able to cooperate to complete the treatment and have complete clinical data.

Exclusion criteria

Exclusion criteria: 1. Preoperative diagnosis of combined calcific tendons; 2. History of previous multiple surgeries on the affected shoulder; 3. Shoulder infection, trauma, fracture, dislocation, etc. within 6 weeks after surgery; 4. Skin ulceration and infection of the affected shoulder, underlying diseases such as cervical spondylosis, severe cardiovascular and cerebrovascular diseases, and patients in pregnancy and lactation; 5. Patients with contraindications to acupuncture or a previous history of acupuncture sickness or rejection of acupuncture treatment.

Design outcomes

Primary

MeasureTime frame
VAS pain score (0-100mm);Active and passive forward flexion, abduction, external rotation and internal rotation of the shoulder joint;UCLA Shoulder Function Score;

Countries

China

Contacts

Public ContactChen Zhenhu

The First Affiliated Hospital of Guangzhou University of Chinese Medicine

936733729@qq.com+86 137 2806 3180

Outcome results

None listed

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