跳至主要内容
临床试验/CTRI/2024/02/063020
CTRI/2024/02/063020已完成4 期

An open–label,single-centric, parallel group,randomized controlled trial to assess effectiveness and safety of topical insulin in wound healing

Dr Meenu Thomas1 个研究点 分布在 1 个国家目标入组 82 人开始时间: 2024年3月4日最近更新:

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
82
试验地点
1
主要终点
To study the effectiveness of topical insulin on wound healing

研究概览

简要总结

Topic: An open –label, single-centric, parallel group, randomized controlled trial to assess effectiveness and safety of topical insulin on wound healing

Aim: To assess effectiveness and safety of topical insulin on wound healing.

Objectives:

To study the effectiveness of topical insulin on wound healing.

To assess the safety of topical Insulin

To compare the topical insulin with normal saline in terms of efficacy and safety

STUDY DESIGN Open –label, single-centric, parallel group, randomized controlled trial

STUDY LOCATION This study will be done on patients visiting the OPD as well as the in-patients General Surgery of Teerthanker Mahaveer Medical College and Research Centre, Moradabad.

STUDY PERIOD This study will be conducted for ≃1.5 to 2 year after the approval from College Research Committee (CRC) and Institutional Ethical Committee (IEC)

Sample size: 41 in each group, 82 total

Inclusion criteria

Age18-65 years old

Either gender

Class 1 and 2 wound classifications as per CDC

Wound surface area 10 (less than 20cm2)

Patients willing to give informed consent

 Exclusion criteria

Pregnancy

Patients on immunosuppressive treatment

Wounds that are complicated (e.g., Bleeding or infection)

Medications that may impact the study’s outcome (NSAIDs etc.)

Cardiovascular illnesses, Peripheral artery disease or Renal and hepatic failure

 Treatment groups

Group A: insulin topical dressing

Group B: Normal saline topical dressing

 Effectiveness assessment

Wound area, depth and pace and amount of granulation tissue. Pain assessment measured at pre-determined time intervals

Safety Assessment

Blood glucose measurement and adverse drug reaction monitoring both spontaneous and checklist

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
None

入排标准

年龄范围
18.00 Year(s) 至 65.00 Year(s)(—)
性别
All

入选标准

  • Age18-65 years old Either gender Class I and II wound classifications as per CDC Wound surface area (less than 20cm2) Patients willing to give informed consent.

排除标准

  • Pregnancy Patients on immunosuppressive treatment Wounds that are complicated (e.g., Bleeding or infection) Medications that may impact the study’s outcome Cardiovascular illnesses, Peripheral artery disease or Renal and hepatic failure.

结局指标

主要结局

To study the effectiveness of topical insulin on wound healing

时间窗: Wound area in mm square shall be measured at day zero then at day 7 and then 14.

次要结局

  • To study effectiveness & safety of topical insulin on wound healing(For effectiveness)

研究者

发起方
Dr Meenu Thomas
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Dr Meenu Thomas

Teerthanker Mahaveer University Medical College and Research Centre

研究点 (1)

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