跳至主要内容
临床试验/CTRI/2019/09/021094
CTRI/2019/09/021094尚未招募2/3 期

Efficacy of light weight mesh repair for uncomplicated inguinal hernia-A randomized clinical trial

DrThanigai sakthi vadivel1 个研究点 分布在 1 个国家目标入组 180 人开始时间: 2019年9月30日最近更新:

试验速览

阶段
2/3 期
状态
尚未招募
发起方
入组人数
180
试验地点
1
主要终点
Light weight mesh is better than heavy weight mesh in terms of postoperative pain,less surgical site infection.

研究概览

简要总结

Inguinal hernias are the most common operative procedure performed by general surgeons, and tension free mesh technique have revolutionized the procedure.Decreased,chronic postoperative pain has become recognized more widely.New mesh products has been introduced now available.Which are considered to be better than conventional polypropylene mesh in terms of postoperative pain and infection rates.

Usage of prosthetic materials decreased the frequency of hernia recurrence,although the chronic pain and surgical site infection will considerably affect the patients quality of life.The pain may be caused by damage to the inguinal nerves, but the surgical site infection is due to the foreign body reaction against the mesh which results in inflammatory response and scar tissue formation. Now a days lightweight meshes are used instead of heavyweight polypropylene mesh.Low mass decreased content of foreign body and large pores characteristic of light weight mesh.So light weight mesh decrease the postoperative pain and decreased tissue reaction.

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Participant Blinded

入排标准

年龄范围
18.00 Year(s) 至 80.00 Year(s)(—)
性别
Male

入选标准

  • Patients willing to participate in the study.
  • All patients of age 18 yrs to 80 yrs with uncomplicated inguinal hernia.

排除标准

  • patients with irreducible inguinal hernia.
  • Recurrent hernia.
  • Strangulated hernia.
  • Benign prostatic hyperplasia.
  • Stricture urethra.
  • Patient refusal to participate in this study.

结局指标

主要结局

Light weight mesh is better than heavy weight mesh in terms of postoperative pain,less surgical site infection.

时间窗: After surgery patients were followed up from postoperative day 3,1 week,1 month to assess for postoperative pain and SSI.

次要结局

未报告次要终点

研究者

发起方
DrThanigai sakthi vadivel
申办方类型
Other [Principal investigator ]

研究点 (1)

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