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临床试验/NCT04937114
NCT04937114Unknown不适用

Efficacy of Unidirectional Barbed Sutures on Various Outcomes in Mucogingival Procedures

SVS Institute of Dental Sciences1 个研究点 分布在 1 个国家目标入组 12 人开始时间: 2021年8月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
12
试验地点
1
主要终点
To assess primary wound closure

研究概览

简要总结

The aim of the study is to compare the efficacy of barbed suture with conventional suture in muco-gingival surgeries.

详细描述

Experimental: Main treatment group, flap will be approximated using conventional, simple continuous suturing with barbed sutures.

Comparator: In patients allocated to control group, flap will be approximated using conventional, simple continuous suturing with conventional sutures.

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
Double (Participant, Care Provider)

入排标准

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

入选标准

  • •Systemically healthy individuals within an age group of 20-50yrs with presence of attached gingiva, shallow vestibule and frenum interfering with the marginal gingiva.

排除标准

  • •Medically compromised patients.
  • •Subjects who underwent radiotherapy or chemotherapy in the past 12 months.

研究组 & 干预措施

Flap will be approximated using conventional, simple continuous suturing with barbed sutures

Experimental

After administration of adequate amount of local anesthesia, planned muco-gingival surgery will be performed and flap will be approximated using conventional, simple continuous suturing with unidirectional barbed sutures.

干预措施: Barbed suture (Procedure)

Flap will be approximated using conventional, simple continuous suturing with conventional sutures

Active Comparator

After administration of adequate amount of local anesthesia, planned muco-gingival surgery will be performed and flap will be approximated using conventional, simple continuous suturing with conventional sutures.

干预措施: Barbed suture (Procedure)

结局指标

主要结局

To assess primary wound closure

时间窗: Baseline to 21days

Primary wound closure and early wound healing by EHS at 7days,14days,21days

次要结局

  • To assess pain(Baseline to 21days)

研究者

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

Dr R Viswa Chandra

Primary Investigator

SVS Institute of Dental Sciences

研究点 (1)

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