Randomized Controlled Trial on the Efficacy and Safety of Xiang Lei Ointment in Diabetic-related Ulcer Management

Overview

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.

Interventions

• Other Xiang Lei Ointment plus Clinical standard treatment protocols
  A therapy for chronic wound healing
• Other Clinical standard treatment protocols
  A therapy for chronic wound healing

Primary outcome measures

• wound area reduction rate [Time frame: From enrollment to the end of treatment at 2 weeks]

Secondary outcome measures (3)

• wound healing rate [Time frame: From enrollment to the end of treatment at 3 weeks]
• Granulation tissue status [Time frame: From enrollment to the end of treatment at 3 weeks]
• wound infection control [Time frame: From enrollment to the end of treatment at 3 weeks]

Eligibility criteria

Inclusion criteria

• 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.

Exclusion criteria

• 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.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation

Randomized

Model

Parallel assignment

Masking

Single blind

Primary purpose

Treatment

Study locations

China · 1 center

• Peking University 3rd Hospital — Beijing

Identifiers

NCT: NCT06841237 · Long2025-DRW-xianglei

Primary sources (government registries)

• ClinicalTrials.gov (US NIH)

View this study on ClinicalTrials.gov ↗