Skip to content

Impact of oral vitamin D in chronic wound patients with Vitamin D Deficiency

Impact of oral vitamin D in chronic wound patients with Vitamin D Deficiency

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200065482
Enrollment
Unknown
Registered
2022-11-06
Start date
2022-11-01
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

Chronic wound

Interventions

Intervention group:Cholecalciferol 6000 IU/d for 8 weeks
Vitamin D deficiency group in the same period:N/A

Sponsors

Guangzhou Red Cross Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Aged >= 18 years, no gender limitation; 2. Wound formation time >= 4 weeks; 3. Liver and kidney functions were normal; No intestinal diseases such as gastrointestinal resection, small intestinal malabsorption; No chronic pancreatitis and no other serious organic disease; 4. Subjects voluntarily, cooperated and signed the informed consent form for this study.

Exclusion criteria

Exclusion criteria: 1. Pregnant woman or feeding women; 2. Cancerous wounds; 3. Untreated osteomyelitis; 4. Patients with long history of smoking or heavy alcohol consumption; 5. Oral supplements, mainly vitamin D, have been available for the past three months.

Design outcomes

Primary

MeasureTime frame
Serum 25 (OH) D;effective wound healing rate;

Secondary

MeasureTime frame
wound volume reduction rate;mean healing day;the score of pressure ulcer scale for healing (PUSH);wound infection rate;

Countries

China

Contacts

Public ContactXiaokun Wu/Haiyan Li

Guangzhou Red Cross Hospital

wuxk@gdpu.email.cn+86 13068695785

Outcome results

None listed

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