Nutritional Supplement on Wound Healing in Diabetic Foot

Last updated: September 18, 2018
Sponsor: Chang Gung Memorial Hospital
Overall Status: Active - Recruiting

Phase

N/A

Condition

Diabetes And Hypertension

Treatment

N/A

Clinical Study ID

NCT03679273
104-9965A3
  • Ages 40-80
  • All Genders

Study Summary

Diabetic foot ulcer (DFU) is the leading cause of non-traumatic limb loss in adult worldwide. One of the major causes of limb loss in patients with DFU is poor wound healing. It is known that nutrition plays a key role in wound healing, not only because of the required calories, but more importantly for collagen remodeling by specific amino acids (arginine, glutamine, and β-hydroxy-β-methylbutyrate).

Nevertheless, few studies have investigated nutritional supplements in patients with poor wound healing of DFU. Difficulties in assessing the severity of a wound and poor adherence to drug and food supplements at home may be important factors for the negative results shown in a most recent prospective randomized controlled trial. The diabetic foot center in Chang Gung Memorial hospital has extensive experience in caring for patients with limb-threatening DFU and we recently reported that poor nutritional status in our patients correlated to poor treatment outcomes. The aim of this study is to evaluate the clinical efficacy and possible molecular mechanisms in nutritional treatment for limb-threatening DFU. A total of 70 patients will be enrolled and randomized into study and control groups. All subjects will receive standard care. Additional amino acid supplements containing arginine, glutamine, and β-hydroxy-β-methylbutyrate or a control (high protein formula powder) will be given orally twice a day for 21 days, and the percentage change in wound size will then be measured. Complete healing time, recurrence or major adverse cardiac events will be recorded during one year of follow up. Data on wound size, nutritional status, and levels of matrix metallopeptidase (MMP)-2, MMP-9, nutrient molecules (measured by ABSOLUTE/DQ P180 KIT (LC MS/MS) will be recorded before and after the nutritional supplementation. In addition, the pioneer factor forkhead box protein A2 (FOXA2) that binds native chromatin and bookmarks genomic regions for transcriptional activity may play a role in nutritional supplements in acute stressed diabetic patients. Therefore, we intend to conduct a pilot study on the for FOXA2 gene in maintaining glucose homeostasis in diabetic foot patients after nutritional interventions.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  1. Subjects will be considered for entry if they are men or non-pregnant women, aged ≥ 40years or ≤ 80 years

  2. a serum albumin level between 2.0 mg/dL and 4.0 mg/dL, had peripheral occlusivearterial disease with an ankle-brachial index (ABI) ≤0.9 or Doppler arterial waveformsthat are biphasic or monophasic

  3. a serum C-reactive protein level ≤ 50 mg/L .

Exclusion

Exclusion Criteria: Subjects will be excluded from the study if they have serious comorbidities such as

  1. pneumonia,

  2. active malignancy, severe renal function impairment (creatinine < 3 mg/dl), heartfailure (NYHA Fc ≥ 3),

  3. liver failure/cirrhosis (Child class B or C),

  4. myocardial infarction in the past 3 months,

  5. wounds complicated with persistent osteomyelitis,

  6. a Charcot deformity,

  7. alcohol/substance abuse,

  8. any mental or physiological condition that may interfere with dietary intake,

  9. history of allergy to any of the ingredients in the supplement,

  10. those who are unable to follow orders or cooperate

Study Design

Total Participants: 70
Study Start date:
October 01, 2018
Estimated Completion Date:
May 15, 2020

Connect with a study center

  • Chang Gung Memorial Hospital

    Taipei, 333
    Taiwan

    Active - Recruiting

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