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临床试验/NCT01598376
NCT01598376已完成不适用

A Prospective Double-blind Interventional Study of Tissue Reaction to Polyglycolic Acid Sutures in Human Skin

The Royal Bournemouth Hospital2 个研究点 分布在 1 个国家目标入组 42 人开始时间: 2010年6月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
42
试验地点
2
主要终点
Suture associated granuloma outer diameter

研究概览

简要总结

Objective

To investigate the tissue reaction produced by implanted polyglactin suture material in normal human skin and to determine the effect of suture gauge on this response.

Design

A prospective, double blind, randomized clinical trial using a novel ethical study design. Both the patient and clinician analyzing the histology were blinded to the suture gauge used.

Participants

A total of 42 consecutive patients presenting to an oculoplastic clinic with involutional entropion and horizontal eyelid laxity, who provided written consent to participate, were enrolled in the study.

Intervention

Patients were randomly allocated to 5/0 or 7/0 Vicryl™ test suture groups. Patient symptoms were alleviated during the wait for definitive surgery by the placement of temporary eyelid everting sutures including a test suture. After 28 days, entropion correction was achieved by a Quickert procedure which includes excision of an eyelid wedge. Histological analysis was carried out, blind to the suture gauge used, on the excised eyelid containing the test suture.

Main outcome measure

Defined histological parameters of suture-related granulomas were measured at multiple levels. Data included granuloma outer diameter, central cellular diameter, giant cell number and area of fibrous coat (calculated from the coat diameter and thickness at multiple levels) and a statistical comparison made between the 5/0 and 7/0 suture gauge groups.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Basic Science
盲法
Double (Participant, Outcomes Assessor)

入排标准

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

入选标准

  • Consecutive patients
  • Involutional lower eyelid entropion
  • Horizontal eyelid laxity associated
  • Informed consent

排除标准

  • Inability to provide informed consent
  • Previous eyelid surgery
  • Poorly controlled diabetes
  • Oral steroid use
  • Addisons disease

结局指标

主要结局

Suture associated granuloma outer diameter

时间窗: 28 days

Histological measurement of suture associated granuloma outer diameter on excised eyelid specimens, average of 6 sections examined

Suture associated granuloma central cellular element diameter

时间窗: 28 days

Histological measurement of suture associated granuloma central cellular element diameter on excised eyelid specimens, average of 6 sections examined

Suture associated granuloma fibrous coat area

时间窗: 28 days

Histological measurement of suture associated granuloma fibrous coat area on excised eyelid specimens, average of 6 sections examined

Suture associated granuloma giant cell number

时间窗: 28 days

Count of giant cells on average of 6 histological sections from excised eyelid specimens

次要结局

未报告次要终点

研究者

发起方
The Royal Bournemouth Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Ben Parkin

Consultant Ophthalmologist

The Royal Bournemouth Hospital

研究点 (2)

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