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临床试验/NCT07535827
NCT07535827已完成1 期

Topical Insulin Insitu-gel as a Wound Healing Accelerator and Anti-inflammatory Agent for Persistent Suppurative Otitis Media in RCT

Deraya University1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2026年3月20日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
入组人数
50
试验地点
1
主要终点
Perforation size

研究概览

简要总结

The objective of the present study was to study the impact of insulin insitu-gel formulation on healing progress after surgical procedures for treatment of dry tympanic membrane perforation for at least three consecutive months. At the beginning, an insulin insitu-gel was prepared from three different polymers compatible with insulin physiochemically and reported to be vain on insulin efficacy or safety. Insulin insitu-gel was prepared using chitosan, polyvinyl alcohol, and Pluronic F127 with glycerol as a penetration enhancer. Selection of an optimized formulation through in situ gel characterization and in vitro drug release kinetics then the formulation was evaluated for healing efficacy on human volunteers in RCT. A randomized controlled clinical study was implemented for clinical evaluation of insitu-gel formulation activity in the Department of Otorhinolaryngology, Minia University Hospital, from March 2026 to May 2026. Perforation healing signs as a primary indicator was followed and reported in three follow-up visits (1 week, 1 month, and 2 months) in addition hearing score pre- and post-surgery as secondary outcomes. Results of a clinical study showed that the healing is significantly superior in the insulin group than in the control group

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Participant)

入排标准

年龄范围
18 Years 至 50 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • aged 18 years or older,
  • with a confirmed diagnosis of tubotympanic CSOM without discharge for at least three months,
  • an intact ossicular chain, normal middle ear mucosa on otoscopic or endoscopic examination,
  • conductive hearing loss indicated by an air-bone gap less than 30 dB

排除标准

  • unfit for general anesthesia,
  • had cervical spine disorders limiting operative positioning,
  • active otorrhea, granulation tissue, or mucosal inflammation

研究组 & 干预措施

placebo group

Placebo Comparator

empty foam was placed after surgery

干预措施: foam (Other)

insulin insitu gel

Experimental

formulated instue-gel was added for foam that placed by ENT surgeon after graft addition

干预措施: Insulin (Humulin) (Drug)

结局指标

主要结局

Perforation size

时间窗: 1 month

endoscopic otoscopy, with graft uptake classified as complete, partial, or failed/reperforated

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Soad Ali

associate professor Daraya university

Deraya University

研究点 (1)

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