Mailuo Shutong Pills for Diabetic Wound Healing: A Multicenter Randomized Trial

NCT07258381 | Not Yet Recruiting DMC

• 1 other identifier: Long2025-DW-ChineseMed：MLST
• Study Type: interventional
• Target: 56
• Locations: 0 countries
• Sites: N/A

Brief Summary

Mailuo Shutong Pills are a Chinese patent medicine approved for market release by the China Food and Drug Administration (CFDA) in 2009. It is formulated by integrating five classical herbal formulas, including Ermiao San, Simiao Yongan Tang, and Zhijing San. Its composition is as follows: Honeysuckle Flower (Jinyinhua) serves as the principal component (Jun herb) for clearing heat and detoxifying; Astragalus Root (Huangqi) for tonifying qi, expelling toxin, and promoting diuresis; Phellodendron Bark (Huangbai), Atractylodes Rhizome (Cangzhu), and Coix Seed (Yiyiren) act as deputy components (Chen herbs) to clear heat and resolve dampness; Chinese Angelica (Danggui), Peony Root (Baishao), and Licorice Root (Gancao) alleviate spasm and pain; Figwort Root (Xuanshen) cools the blood, clears heat, drains fire, detoxifies, and softens hard masses. Leeches (Shuizhi), Centipede (Wugong), and Scorpion (Quanxie) serve as assistant components (Zuo herbs) to invigorate blood, resolve stasis, attack toxicity, dissipate nodules, and unblock collaterals to relieve pain. Licorice Root (Gancao) also harmonizes the various components in the formula as the envoy component (Shi herb). The complete formula possesses the effects of clearing heat and detoxifying, dissolving stasis and unblocking collaterals, and dispelling dampness and reducing swelling. It is indicated for various conditions differentiated in Traditional Chinese Medicine (TCM) as presenting with a pattern of dampness-heat and stasis obstruction, such as superficial thrombophlebitis and deep vein thrombosis in the non-acute stage. Some studies suggest that Mailuo Shutong Pills may have a positive effect in the field of wound healing, for example, by significantly reducing the release of inflammatory mediators such as IL-1β, IL-6, CRP, and TNF-α caused by inflammatory diseases \[11-13\], and accelerating the healing of diabetic foot wounds \[14\]. Clinical guidelines, including the "Clinical Application Guide for Chinese Patent Medicines - Diabetes Volume" from the Diabetes Branch of the China Association of Chinese Medicine and the "Integrated Traditional Chinese and Western Medicine Diagnosis and Treatment Guidelines for Diabetic Foot" from the Chinese Medical Doctor Association, recommend Mailuo Shutong Pills for the treatment of diabetic foot ulcers \[15\]. However, the current related evidence-based medical evidence is insufficient. We have also observed that the adjunctive use of Mailuo Shutong Pills does not guarantee a shortened healing time for all patients with diabetic wounds. From a TCM perspective, the presence of a dampness-heat and stasis obstruction pattern is a key factor determining the efficacy of adjunctive Mailuo Shutong therapy. For Western medicine practitioners, tongue diagnosis presents a practicable factor for assessing pattern manifestation. Therefore, based on differences in patient patterns and using tongue appearance as an inclusion/exclusion criterion, to screen for the indications of Mailuo Shutong Pills combined with existing standard treatment for diabetic wounds constitutes an effective technical approach to address the aforementioned issues. Consequently, this study aims to explore the indications for Mailuo Shutong Pills in diabetic wounds and obtain evidence-based medical evidence for its clinical efficacy within an integrated Chinese-Western medicine approach. Furthermore, to enhance the study's external validity and participant recruitment efficiency, thereby accelerating the research progress, this study is designed as an exploratory trial conducted across multiple centers.

Conditions

Diabetic Wound; Chronic Wound Care

Keywords

diabetic wound; chronic wound care

Outcome Measures

Primary Outcomes (1)

• wound area reduction rate

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

  Day14 ± 2

Secondary Outcomes (4)

• wound healing rate

  Day14 ± 2

• Granulation tissue status

  Day 0/Day 14 ± 2

• wound infection control

  Day 0/Day 14 ± 2

• Tongue appearance

  Day 0, Day 7±2 and Day 14±2

Study Arms (2)

Experimental group

EXPERIMENTAL

Based on the clinical standard treatment plan, oral administration of Maoluo Shutong Pills was administered for 2 weeks

Drug: Mailuo Shutong Pills

Control group

SHAM COMPARATOR

the clinical standard treatment plan

Drug: Blank control

Interventions

Mailuo Shutong Pills DRUG

a medicine that treating Diabetic Wounds with Damp-Heat Toxin Accumulation Syndrome

Experimental group

Blank control DRUG

Blank control

Control group

Eligibility Criteria

• Age: 18 Years - 80 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• a confirmed diagnosis of type 1 or type 2 diabetes mellitus;
• the type of wound is an ulcer, with an ulcer area ranging from 1 to 40cm ²;
• the wound etiology is diabetic, mainly abnormalities in blood glucose, resulting in poor or prolonged healing and requiring standard wound therapy;
• The traditional Chinese medicine diagnosis is Damp-Heat Toxin Accumulation Syndrome;
• voluntary participation in the study and signing of an informed consent form.

You may not qualify if:

• Diagnosis of a Cold Pattern according to Traditional Chinese Medicine (TCM) differentiation, manifested as: pale, enlarged, and tender tongue with a white, moist or glossy coating; pallor; pale lips; aversion to cold with a preference for warmth; and loose stools.
• Pregnancy or lactation.
• Presence of severe, uncorrected systemic diseases, such as acute myocardial infarction, heart failure, hepatitis, shock, or respiratory failure.
• Active bleeding within the wound that prevents the implementation of standard wound care.
• Severe laboratory abnormalities: serum albumin \< 20 g/L; hemoglobin \< 60 g/L; or platelet count \< 50 × 10⁹/L.
• Diagnosis of advanced malignant tumor.
• Active phase of an autoimmune disease.
• History of hypersensitivity to Mailuo Shutong Pills or Mailuo Shutong Granules.
• Inability to cooperate with the study procedures or presence of psychiatric disorders.
• Any other condition considered by the investigator as a clear, unmodifiable factor adversely affecting wound healing, making the candidate unsuitable for the study or unable to comply with the study requirements.

Sponsors & Collaborators

• Peking University Third Hospital: lead

Central Study Contacts

Long Zhang Executive Deputy Director, Medical Doctor

CONTACT

+86 010-82266699; longzh2000@163.com

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: Head of Wound Healing Center

Model Details: Randomized control trial

Study Record Dates

• First Submitted: November 14, 2025
• First Posted: December 2, 2025
• Study Start: December 1, 2025
• Primary Completion (Estimated): December 1, 2026
• Study Completion (Estimated): December 1, 2027
• Last Updated: December 2, 2025

Record last verified: 2025-11