Randomized Controlled Trial on the Efficacy and Safety of Xiang Lei Ointment in Diabetic-related Ulcer Management
1 other identifier
interventional
56
1 country
1
Brief Summary
Diabetes is one of the major chronic diseases. Diabetic ulcers are important adverse outcomes of diabetes. Approximately 80% of lower - limb amputations are caused by diabetic foot ulcers, which are the main causes of disability and death among patients. Moreover, it places a huge burden on the medical insurance system. Currently, there are western medicine treatment guidelines for diabetic foot, yet the clinical efficacy is less than satisfactory. The amputation rate caused by diabetic foot ulcers continues to rise every year. There is an urgent clinical need for novel and effective intervention measures to address this disease. Macrophages are important cells involved in the inflammatory and proliferative phases of wounds, playing a crucial role in wound repair and reconstruction. Diabetes can cause wounds to remain in the pro - inflammatory stage continuously, leading to the aggregation of M1 macrophages and preventing their timely transformation into the pro - proliferative and repair stage. As a result, wounds exhibit persistent chronic inflammation and delayed tissue proliferation or remodeling. Xianglei Tangzu Ointment is a natural medicine approved for marketing by the National Medical Products Administration in November 2023. Its ingredients include Pogostemon cablin extract and asiaticoside. Research shows that the plant components in Xianglei Tangzu Ointment can promote the transformation of M1 macrophages into M2 macrophages, thereby reducing the inflammatory response and accelerating the proliferative repair of diabetic wounds. It has achieved certain curative effects in the clinical treatment of promoting wound healing. In order to use Xianglei Tangzu Ointment more precisely, accumulate clinical evidence - based medicine evidence, and explore the effectiveness and safety of Xianglei Tangzu Ointment in treating diabetic ulcers under the guidance of the chronic wound staging theory, clinical evidence - based medicine evidence needs to be obtained.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Apr 2025
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
February 18, 2025
CompletedFirst Posted
Study publicly available on registry
February 24, 2025
CompletedStudy Start
First participant enrolled
April 10, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 15, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
February 15, 2027
March 2, 2026
February 1, 2026
1.3 years
February 18, 2025
February 26, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
wound area reduction rate
Pre-treatment area minus post-treatment area, then divided by pre-treatment area
From enrollment to the end of treatment at 2 weeks
Secondary Outcomes (3)
wound healing rate
From enrollment to the end of treatment at 3 weeks
Granulation tissue status
From enrollment to the end of treatment at 3 weeks
wound infection control
From enrollment to the end of treatment at 3 weeks
Study Arms (2)
test group
EXPERIMENTALClinical standard treatment protocols plus Xiang Lei Ointment
control group
SHAM COMPARATORClinical standard treatment protocols
Interventions
A therapy for chronic wound healing
Eligibility Criteria
You may qualify if:
- a confirmed diagnosis of type 1 or type 2 diabetes mellitus that meets the standard World Health Organization definition, with blood glucose controlled prior to enrolment and a glycated haemoglobin HbA1c level of less than 10%;
- the type of wound is an ulcer;
- the wound etiology is diabetic, mainly abnormalities in blood glucose, resulting in poor or prolonged healing and requiring standard wound therapy;
- the staging of the wound is in the granulation phase;
- voluntary participation in the study and signing of an informed consent form.
You may not qualify if:
- acute heart attack, heart failure, hepatitis, shock, expiratory failure and other serious diseases that have not been corrected;
- uncontrolled blood glucose, fasting blood glucose \> 15 mmol/L and glycated haemoglobin \> 12%;
- active bleeding in the wound, which does not allow the implementation of the conventional basic treatment plan;
- serum albumin \< 20 g/L; haemoglobin \< 60 g/L; platelets \< 50 x 109/L;
- a state of disseminated infection that is being or will be treated with antibiotics
- patients with advanced malignant tumours;
- active autoimmune disease;
- previous allergy to topical human granulocyte macrophage stimulating factor gel (Jinfuning);
- inability of the patient to co-operate or mental disorder;
- in the judgement of the investigator, the subject has a clearly irremovable cause of wound healing, is unsuitable for the study or is unable to comply with the requirements of the study.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Peking University 3rd Hospital
Beijing, Beijing Municipality, 100191, China
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor, Head of Wound Healing Center
Study Record Dates
First Submitted
February 18, 2025
First Posted
February 24, 2025
Study Start
April 10, 2025
Primary Completion (Estimated)
July 15, 2026
Study Completion (Estimated)
February 15, 2027
Last Updated
March 2, 2026
Record last verified: 2026-02
Data Sharing
- IPD Sharing
- Will not share