Clinical Study of Methylene Blue - Mediated Photodynamic Therapy for Diabetic Lower Limb Ulcer

Sponsor
Chongqing Medical University (Other)
Overall Status
Unknown status
CT.gov ID
NCT03222544
Collaborator
(none)
60
1
2
14
4.3

Study Details

Study Description

Brief Summary

The investigators designed this prospective, randomized control study to confirm the efficacy and safety of methylene blue - mediated photodynamic therapy for diabetic lower limb ulcer and to explore its mechanism.

Condition or Disease Intervention/Treatment Phase
  • Combination Product: methylene blue
  • Combination Product: Photon therapy instrument
N/A

Detailed Description

OBJECTIVE- Infection is associated with poor healing of diabetic lower limb ulcer. Diabetic lower limb ulcer are often lower extremity vascular stenosis or occlusion, poor blood supply, making local ulcer local antibacterial drugs difficult to effectively reach and distribution, resulting in systemic antibacterial efficacy is limited, and easy to induce bacterial resistance at the same time . In recent years, the incidence of clinical multidrug-resistant bacteria increased, increasing the difficulty and cost of treatment.

The current study attempts to identify whether the photodynamic therapy (PDT) would kill the surface of ulcer bacteria and promote ulcer healing, and explore the mechanism of methylene blue-mediated photodynamic therapy for diabetic lower limb ulcer RESEARCH DESIGN AND METHODS-This study evaluated six clinical indicators: diabetic foot ulcer area reduction rate, inflammation control rate, Local bacterial load, the dose and use time of antibiotics, adverse reaction rate, bacterial biofilm,local neutrophil extracellular traps. The efficacy and safety of PDT could be confirmed if the clinical indicators of PDT group is better than the control group. In this study, three methods were used to investigate the mechanism of -methylene blue mediated photodynamic therapy for diabetic lower limb ulcer: a comparison of the bacterial load, bacterial biofilm,local neutrophil extracellular traps of the ulcer immediately pre-treatment and immediately,1-week ,2 week,1 momth post-treatment ; EXPECTED RESULTS-The investigators will expect that methylene blue-mediated photodynamic therapy could kill bacteria on the surface of diabetic lower limb ulcer and accelerate wound healing.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
60 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Care Provider, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Efficacy and Safety of Methylene Blue -Mediated Photodynamic Therapy for Diabetic Lower Limb Ulcer : a Randomized Controlled Study
Anticipated Study Start Date :
Apr 29, 2019
Anticipated Primary Completion Date :
Apr 29, 2020
Anticipated Study Completion Date :
Jun 29, 2020

Arms and Interventions

Arm Intervention/Treatment
Experimental: Photodynamic Therapy

The photosensitizer, methylene blue, is applied topically to the ulcer surface and the ulcer was shielded from light for 15 min. Then the ulcer area is illuminated using a photon therapy instrument for 20 minutes. Photodynamic therapy is applied once a day for a total of seven times.

Combination Product: methylene blue
Continue treatment after 5mins suspension if the patient feels that the local temperature is too high to stand

Active Comparator: Photon therapy

The placebo is applied topically to the ulcer surface and the ulcer was shielded from light for 15 min. Then the ulcer area is illuminated using a photon therapy instrument for 20 minutes. Photon therapy is applied once a day for a total of seven times.

Combination Product: Photon therapy instrument
Continue treatment after 5mins suspension if the patient feels that the local temperature is too high to stand

Outcome Measures

Primary Outcome Measures

  1. Change from baseline (Ulcer area)in the diabetic lower limb ulcer at day 7 [Baseline and day 7]

    Changes of ulcer area before and after treatment

  2. Change from baseline (immediately before the first treatment) in the bacterial load of the ulcer at one hour (immediately after the first treatment) [Baseline and (immediately after the first treatment),day 7,14,21,28]

    Changes of local bacterial load before and after treatment

  3. Change from baseline(bacterial biofilm) [Baseline and day 7,14,21,28]

    Changes of local bacterial biofilm before and after treatment

Secondary Outcome Measures

  1. The dose of antibiotics [7 days during treatment]

    Dosage of antibiotics during treatment

  2. The time of antibiotics [7 days during treatment]

    Antibiotic use time during treatment

  3. Adverse events [7 days during treatment]

    including pain,redness, and swelling

  4. A comparison of local NET neutrophil extracellular traps before the first treatment and after the tenth treatment [Baseline and day 7,14,21,28]

    Fluorescence intensity and area of local NET

  5. Inflammation control rate [7 days during treatment]

    Duration of inflammation

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
    1. Understand the whole test process, voluntary and signed informed consent form.
    1. Men and women aged 18 to 80 years old.
    1. Diagnosed with diabetic lower limb ulcer.
    1. Ulcer duration> 1 month of wagner grade Ⅱ, Ⅲ subjects.
    1. An ulcer area ≤100 cm² or of linear dimension ≤ 10 cm.
Exclusion Criteria:
    1. Diagnosis of systemic infection or any concomitant infection that would require treatment with an additional antimicrobial agent.
    1. Pregnant or lactating women.
    1. Wagner grade Ⅰ, Ⅳ, Ⅴ subjects.
    1. Patients with a peripheral vascular disease require immediate revascularization, and/or an ankle brachial systolic blood pressure (SBP) index<0.5 in the infected limb.
    1. Patients with inappropriate health to participate as determined by the principal investigators.
    1. Patients in the hepatitis A, hepatitis B, AIDS, tuberculosis and other infectious diseases of the active period.

Contacts and Locations

Locations

Site City State Country Postal Code
1 The First Affiliated Hospital of Chongqing Medical University Chongqing Chongqing China 400016

Sponsors and Collaborators

  • Chongqing Medical University

Investigators

  • Principal Investigator: Qingfeng Cheng, PhD, the First Affiliated Hospital, Chongqing Medical University, China

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Cheng Qing-feng, Associate professor, Chongqing Medical University
ClinicalTrials.gov Identifier:
NCT03222544
Other Study ID Numbers:
  • PDT2017
First Posted:
Jul 19, 2017
Last Update Posted:
Apr 23, 2019
Last Verified:
Apr 1, 2019
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Cheng Qing-feng, Associate professor, Chongqing Medical University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 23, 2019