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

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-80
SponsorPeking University Third Hospital

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

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;

Disqualifiers

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;

Trial design

Design model

Parallel

Treatments tested in this trial

  • Xiang Lei Ointment plus Clinical standard treatment protocols

    Other intervention

    A therapy for chronic wound healing

  • Clinical standard treatment protocols

    Other intervention

    A therapy for chronic wound healing

Treatment groups

56 Participants
are divided into 2 treatment groups
Group A: test groupExperimental treatment 1 intervention
Group B: control groupSham comparator 1 intervention

Trial outcomes

Primary outcomes

1

wound area reduction rate

Pre-treatment area minus post-treatment area, then divided by pre-treatment area

Time frame
From enrollment to the end of treatment at 2 weeks

Secondary outcomes

1

wound healing rate

Percentage of healed wounds to total cases by D21

Time frame
From enrollment to the end of treatment at 3 weeks
2

Granulation tissue status

They were classified as healthy granulation, inflammatory granulation, infected granulation, oedematous granulation, and aged granulation. D0/D14/D21, wound granulation tissue status was recorded separately

Time frame
From enrollment to the end of treatment at 3 weeks
3

wound infection control

0 points for no infection, 1 point for reduction of localised infection; 2 points for maintenance or exacerbation of localised infection; 3 points for disseminated infection; record D0/D14/D21, the status of the wound infection and record the scoring results respectively

Time frame
From enrollment to the end of treatment at 3 weeks

Other outcomes

Sponsors and contacts

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