biological drilling at 50 RPM
ProcedureBiological drilling (no irrigation) at 50 rpm for all sequential drills.
NCT Number: NCT07474454
This randomized controlled clinical trial aims to evaluate the effect of different biological drilling speeds (50, 150, and 300 rpm) during implant osteotomy preparation in the mandible on marginal bone level changes and implant stability. Thirty-nine patients requiring a single dental implant in the mandible will be randomly allocated into three groups according to drilling speed. All implants will be placed using a biological drilling protocol without irrigation. Implant stability will be measured using resonance frequency analysis at implant placement and follow-up visits. Marginal bone levels will be evaluated radiographically using standardized periapical radiographs during the follow-up period up to 12 months. The study aims to determine whether different low-speed drilling protocols influence peri-implant bone remodeling and implant stability.
Trial opening soon.
Get Notified20 year–60 year
All sexes
Interventional
Not applicable
This randomized parallel-group clinical trial will investigate the influence of different biological drilling speeds on radiographic marginal bone level changes and implant stability in mandibular dental implant placement.
Thirty-nine partially edentulous adult patients requiring a single implant in the mandible will be recruited from the outpatient clinic of the Department of Oral and Maxillofacial Surgery, Faculty of Dentistry, Cairo University. Eligible participants will be randomly assigned to one of three groups according to drilling speed used during osteotomy preparation: 50 rpm, 150 rpm, or 300 rpm.
Implant site preparation will be performed using the same sequential drilling protocol and implant system in all groups. Biological drilling will be performed without irrigation, with careful control of drilling pressure and intermittent drilling to minimize thermal trauma.
Implant stability will be measured using resonance frequency analysis (RFA) at implant placement and during follow-up visits. Radiographic assessment of marginal bone levels will be conducted using standardized periapical radiographs obtained using the paralleling technique. Radiographic measurements will be performed at baseline and during follow-up visits up to 12 months.
The primary outcome of the study will be marginal bone level changes measured radiographically in millimeters. The secondary outcome will be implant stability expressed as Implant Stability Quotient (ISQ) values.
The results of this study may help identify the optimal biological drilling speed that preserves bone vitality while maintaining adequate implant stability and favorable peri-implant bone remodeling.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Biological drilling (no irrigation) at 50 rpm for all sequential drills.
Biological drilling (no irrigation) at 150 rpm for all sequential drills.
Biological drilling (no irrigation) at 300 rpm for all sequential drills.
Time frame: Baseline (Surgery) and 12 months postoperatively.
Change in bone level measured from a fixed implant reference point to the crestal bone level using periapical radiographs.
Time frame: At time of insertion and 3 months postoperatively.
Measured via Resonance Frequency Analysis (RFA) to obtain Implant Stability Quotient (ISQ) values.
Cairo University
Other
Radiographic Assessment of Mandibular Biological Drilling at Different Drilling Speeds: A Randomized Clinical Trial
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT07475416
Edentulism, Mouth Diseases
View Trial DetailsNCT07468747
Edentulism, Mouth Diseases
Ajman, United Arab Emirates
View Trial DetailsNCT07633665
Edentulism, Mouth Diseases
Konya, Turkey (Türkiye)
View Trial DetailsNCT06287346
Edentulism, Mouth Diseases
Boulder, Colorado, United States
View Trial Details