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Clinical Efficacy of Vitamin D in Patients with Ratator Cuff Injury and Vitamin D Deficiency: A Randomized Controlled Trial.

Clinical Efficacy of Vitamin D in Patients with Ratator Cuff Injury and Vitamin D Deficiency: A Randomized Controlled Trial.

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500099477
Enrollment
Unknown
Registered
2025-03-24
Start date
2025-03-26
Completion date
Unknown
Last updated
2025-03-31

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

Conditions

Ratator Cuff Injury

Interventions

Group A:Therapeutic regimen: Injection into the affected shoulder joint cavity combined with periarticular nerve block (1% lidocaine 60mg + mecobalamin 0.5mg + compound betamethasone 5mg + normal sali
Group B:Therapeutic regimen: Injection into the affected shoulder joint cavity combined with periarticular nerve block (1% lidocaine 60mg + mecobalamin 0.5mg + compound betamethasone 5mg+ normal salin

Sponsors

Affiliated Hospital of Xuzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Patients meeting the diagnostic criteria for rotator cuff injury, with persistent pain in the affected shoulder for >3 months, Zlatkin classification type I-II, aged 18-75 years, Numeric Rating Scale (NRS) score >=4, BMI 18-24, and serum 25-hydroxyvitamin D [25(OH)D] level <75 nmol/L (30 ng/mL).

Exclusion criteria

Exclusion criteria: 1. Presence of other significant shoulder pathologies (e.g., fractures, rheumatic diseases); 2. History of neck or shoulder surgery; 3. Patients currently taking vitamin D supplements; 4. Conditions such as hyperphosphatemia with renal rickets, hypervitaminosis D, hypothyroidism/hyperthyroidism; 5. Patients with primary or secondary hyperparathyroidism;6.Renal insufficiency or hypercalcemia; 7. Pregnant or lactating women; 8. Participation in other clinical trials currently or within the past 12 weeks; 9. Inability to comprehend study scales/questionnaires or refusal to participate

Design outcomes

Primary

MeasureTime frame
pain score;

Secondary

MeasureTime frame
shoulder function;sleep quality;inflammatory factor levels;Depression Index;anxiety index;the level of Vitamin D;

Countries

China

Contacts

Public ContactYin Qin

Department of Pain,Affiliated Hospital of Xuzhou Medical University

yinqin@126.com+86 151 6211 4321

Outcome results

None listed

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