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临床试验/NCT05218941
NCT05218941终止不适用

New IMPLANTARY SURGERY Protocol ASSISTED BY PASSIVE ROBOTIQUE: Pilot Study

University Hospital, Toulouse1 个研究点 分布在 1 个国家目标入组 15 人开始时间: 2023年1月23日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
终止
入组人数
15
试验地点
1
主要终点
Pain assessment

研究概览

简要总结

The use of a passive robotic system allows the practitioner to widen the field of indications of flapless surgical access to the implant with an increased operative security and the possibility of an operative modification of the surgical protocol.

详细描述

In recent decades, the placement of dental implants has become a common procedure for the rehabilitation of partially or completely edentulous patients. The placement of implants requires good visibility of the bone support to avoid accidents such as bone fenestration. This is why, except in very favourable cases where the bone crest is wide, unconcavated and with an ideal periodontal support, it was until then necessary to proceed with a flap before placing the implant. This invasive surgical protocol necessary for implant placement with good visual access has negative parameters such as :

  • detachment of the periosteum and therefore risk of bone resorption
  • longer intervention time
  • need for sutures
  • post-operative pain. On the other hand, flapless techniques, which respect the periosteum and periodontium, offer simpler surgical outcomes, reduced risk of bleeding and infection, less bone resorption, and overall better healing. However, the absence of an access flap to the implant site requires special anatomical conditions to avoid any risk of bone fenestration during drilling, and this technique is directly related to the operator's experience. Increasing the number of cases treated by flap-free implant surgery with increased safety is now possible thanks to computer-assisted surgery and passive robotics.

The main objective is to compare the patient's post-operative pain outcomes between passive robotic implant surgery and conventional implant surgery.

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
None

入排标准

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

入选标准

  • •Patient at least 21 years old
  • •Favorable diagnosis of implant placement regardless of technique (ambivalence clause)
  • •Radiological situation with sufficient bone volume but requiring a muco-gingival flap or the help of passive robotics.
  • •Affiliated or beneficiary of a social security
  • •Signed informed consent

排除标准

  • •Patient eligible for one or more implants and having a broad bone crest, with no marked concavity, and covered with a sufficient amount of keratinized attached gum.
  • •Patient with limited oral opening
  • •Patient with contraindications to implant placement (valve prostheses, unbalanced diabetes)
  • •Photosensitive epileptic patient
  • •Patient refusal to participate in the study
  • •Pregnant or breastfeeding woman
  • •Patients under guardianship or curatorship

研究组 & 干预措施

Passive robotic group

Experimental

Implant surgery without flap assisted by passive robotics

干预措施: Implant surgery assisted by passive robotics (Procedure)

Control group

Active Comparator

Implant surgery with flap

干预措施: Conventional implant surgery (Procedure)

结局指标

主要结局

Pain assessment

时间窗: 24 hours

Pain assessment according to a visual analogue scale ranging from 0 to 10

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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