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Clinical Evaluation and Generalized Application of Qing-Hua-Bu Three Dynamic Sequential Therapy of Diabetic Ulcer

Clinical Evaluation and Generalized Application of Qing-Hua-Bu Three Dynamic Sequential Therapy of Diabetic Ulcer

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03574935
Enrollment
150
Registered
2018-07-02
Start date
2018-07-01
Completion date
2019-10-30
Last updated
2018-07-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diabetic Foot, Ulcer, Skin

Keywords

Qing-Hua-Bu, Dynamic sequential treatment, Clinical evaluation, Generalized application

Brief summary

This project is based on investigator team's ten year experience on diabetic ulcer and goes on further developing basic research and concluding clinical experience. The investigator team has recently developed Remove stasis to generate granulation tissue into Remove slough to generate granulation tissue. Investigators have applied the principle of Remove stasis in the medium and later stage of treatment to make Remove slough-Eliminate stasis-Generate granulation tissue become the basic principle of three-stage sequential treatment. Investigators will further conclude Chinese medicine therapy in the stage of Qing-Hua-Bu and evaluate safety, applicability and availability of it. Therefore, the research can help improve clinical diagnosis and treatment technique and transfer the study result of Chinese medicine experience on diabetic ulcer.

Detailed description

Aim: Under guidance of Clear pus-Remove stasis-Supplement muscles theory, to observe clinical effectiveness of dynamic Chinese external therapy of Qing-Hua-Bu in treating diabetic ulcer and partially explain potential wound healing mechanism. Method: Clinical observation: To adopt the design method of open and parallel control test and include 150 diabetic ulcer patients. The treatment group was supplied with external clearing heat, removing stasis and supplementing deficiency Chinese medicine, while the control group was supplied with sulfadiazine silver cream, furacilin solution and bovine basic fibroblast growth factors (b-FGF) spray. To perform the dressing change for wound every day and persist in dressing change for two months. To record dynamic wound healing progress by digital camera. After finishing course, to compare wound healing, pus, exudate, granulation tissues and epithelial tissues and analyze these data by SPSS22.0.

Interventions

DRUGExternal Chinese medicine

External Chinese medicine: For patients in the treatment group, they will accept one of three specific External Chinese medicine according to their lesions and corresponding syndromes: 1. Chinese herb of Clear heat-Remove dampness-Detoxicate for patients belong to heat syndrome; 2. Chinese herb of Activating blood-Removing stasis for patients belong to stasis syndrome; 3. Chinese herb of Supplement deficiency-Generate muscles for patients belong to deficiency syndrome.

DRUGExternal Western medicine

For patients in the control group, they will accept one of three specific external Western medicine according to their lesions: 1.Ethacridine Lactate Solution(lesions with much effusion); 2.1% Sulfadiazine Silver Cream(lesions with infection); 3.rb-bFGF(lesions with no slough and look clear).

Sponsors

Shanghai Yueyang Integrated Medicine Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

1. accord with standard of syndrome differentiation of traditional Chinese medicine and western medicine diagnostic criteria; 2. age between 18-65 years old, gender, ethnic unlimited; 3. agreed to participate in clinical trials can observe and cooperate with the visitor on schedule; 4. sign the informed consent form and mark the date; 5. If the patients are in the child-bearing period, they should accept the test of HCG and the result should be negative;

Exclusion criteria

1. systematic application of steroids or immunosuppressor within 2 weeks; 2. be allergic to any contents of known studied medicine; 3. experiment results that may influence patients' safety; 4. women within gestation period,suckling period or planning to gestation period; 5. patients with severe heart, liver or kidney diseases; 6. have received other studying medicine or taken part in other clinical experiments; 7. cannot cooperate with the study for any reasons,such as language understanding and not able to see the doctors; 8. other situations or diseases that researchers think may bring obvious risks to patients or interfere with the study results. 9. cancer ulcer; tuberculotic ulcer;radioactive ulcer

Design outcomes

Primary

MeasureTime frameDescription
Wound healing rateup to 56 days after treatmentTo perform the dressing change for wound every day and persist in dressing change for two months. To record dynamic wound healing progress by digital camera. After finishing course, to compare wound healing, pus, exudate, granulation tissues and epithelial tissues and analyze these data by SPSS22.0.

Contacts

Primary ContactFulun Li
drlifulun@163.com0086-021-65162629
Backup ContactMinfeng Wu
996392167@qq.com0086-021-50690332

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026