NCT06841237

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

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
56

participants targeted

Target at P25-P50 for not_applicable

Timeline
10mo left

Started Apr 2025

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress58%
Apr 2025Feb 2027

First Submitted

Initial submission to the registry

February 18, 2025

Completed
6 days until next milestone

First Posted

Study publicly available on registry

February 24, 2025

Completed
2 months until next milestone

Study Start

First participant enrolled

April 10, 2025

Completed
1.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 15, 2026

Expected
7 months until next milestone

Study Completion

Last participant's last visit for all outcomes

February 15, 2027

Last Updated

March 2, 2026

Status Verified

February 1, 2026

Enrollment Period

1.3 years

First QC Date

February 18, 2025

Last Update Submit

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

EXPERIMENTAL

Clinical standard treatment protocols plus Xiang Lei Ointment

Other: Xiang Lei Ointment plus Clinical standard treatment protocols

control group

SHAM COMPARATOR

Clinical standard treatment protocols

Other: Clinical standard treatment protocols

Interventions

A therapy for chronic wound healing

control group

A therapy for chronic wound healing

test group

Eligibility Criteria

Age18 Years - 80 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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

RECRUITING

MeSH Terms

Conditions

Wound Infection

Condition Hierarchy (Ancestors)

Infections

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: Multicenter, Randomized, Open-lable
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

Locations