Topical Insulin Insitu-gel as a Wound Healing Accelerator and Anti-inflammatory Agent for Persistent Suppurative Otitis Media in RCT
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
- 是
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
empty foam was placed after surgery
干预措施: foam (Other)
insulin insitu gel
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
Soad Ali
associate professor Daraya university
Deraya University
