跳至主要内容
临床试验/CTRI/2024/01/061562
CTRI/2024/01/061562尚未招募2 期

Efficacy of Platelet-Rich Plasma and Platelet-Rich Fibrin in Diabetic Foot Ulcer- A Randomised, parallel group active comparator trial - NI

Chahat Bansal0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
2 期
状态
尚未招募
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • Age more than 18 years and less than 70years
  • Both male and female group
  • Documented Diagnoses of Diabetes Mellitus
  • Ulcer Characteristics
  • Ulcer size more than 0.5cm2 and less than 20cm2
  • Ulcer site Plantar surface of foot
  • Ulcer duration more than 4 weeks
  • UTS Grade 1A 1B 1C,2A 2B or 2C
  • Ulcers with absent or mild infection according to IWGDF or IDSA grading
  • Palpable dorsalis pedis artery anterior tibial artery and posterior tibial artery or
  • ABI more than0.8 or duplex ultrasound with biphasic waveform below the knee and preserved peak systolic velocity
  • No planned revascularization procedure or vascular surgery with the last or next 30 days from the day of eligibility screening
  • Plantigrade foot
  • Subjects and caregivers willing and able to comply with all the study procedures and visits and has reasonable expectations of completing the study
  • Informed Consent

排除标准

  • Ulcers with moderate or severe infection according to IWGDF grading requiring active surgical debridement or intravenous antibiotics
  • Ulcers of grade 1D 2D 3A 3B 3C or 3D according to University of Texas staging for DFUs
  • Ulcers due to underlying Charcot foot
  • Ulcer on foot other than plantar surface
  • Evidence of osteomyelitis on any part of the limb
  • Evidence of gangrene on any part of the affected limb
  • Bilateral diabetic foot ulcers
  • ankle brachial index less than 0.8 or non-palpable ATA PTA DPA
  • haemoglobin less than 10g per dl
  • platelet count less than 150000 per dl
  • Chronic kidney disease with eGFR less than 30 ml per min per 1.73m2 or Urine albumin creatinine ratio of more than 300 mg per g
  • Presence of varicosities or deep vein thrombosis in the affected limb
  • immunodeficiency
  • coagulopathies
  • Active malignancy
  • Chronic steroid use or immunosuppressive agents within the last 3 months prior to enrolment
  • Participation in another study pertaining to advanced wound closure product
  • Use of growth factor therapy autologous platelet-rich plasma gel dermal substitute negative pressure wound therapy within two weeks of study enrolment

研究者

发起方
Chahat Bansal

相似试验