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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.
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.
Age
21 - No limit years
Sex
ALL
Healthy Volunteers
No
Toulouse University Hospital
Toulouse, France
Start Date
January 23, 2023
Primary Completion Date
December 2, 2024
Completion Date
December 2, 2024
Last Updated
May 21, 2025
15
ACTUAL participants
Implant surgery assisted by passive robotics
PROCEDURE
Conventional implant surgery
PROCEDURE
Lead Sponsor
University Hospital, Toulouse
NCT05500755
NCT07019428
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT06449391