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Computer Guided Versus Conventional Surgical Removal of Deeply Impacted Mandibular Third Molar With Preservation of External Oblique Ridge

Computer Guided Versus Conventional Surgical Removal of Deeply Impacted Mandibular Third Molar With Preservation of External Oblique Ridge

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03447067
Enrollment
18
Registered
2018-02-27
Start date
2018-03-28
Completion date
2018-07-30
Last updated
2018-02-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Impacted Third Molar Tooth

Brief summary

in patent have deeply impacted lower third molar ,dose computer guided enhance surgical outcome versus conventional surgical remove of wisdom teeth

Detailed description

P- Patient with deeply impacted mandibular molar I- Computer guided surgical cutting stent C- Conventional extraction O- Clinical outcome sound radiographic outcomes primary outcome \- pain : each patient well be asked to rate current and worst pain intensity on visual analogue scale (VAS ) of 0-10 with Zero being no pain and Ten corresponds to the worst pain. Secondary outcome * evaluation of maximum inter incisal opening: assessment of MMO will be performed by measuring the distance in mm between the incisal edges of the upper and lower central incisor by using tape graduated method. * evaluation of edema throw use nylon thread.

Interventions

PROCEDUREcomputer guided surgical

has three cutting guided plane for identify the position of place of the third molar, it have beveled cut for stability after remove the teeth and placing the bony window

PROCEDUREConventional surgery

Low speed motor with surgiacl round burs and surgical fissure for removal a covering bone with decapitation and guttering formation

DEVICECBCT

For measuring the bone removeal

Sponsors

Alaadden Mahmoud Abu Al Enein
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
16 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* patient with deeply impacted mandibular third molar * patients should be free from any systematic disease that affect normal healing

Exclusion criteria

* -Patient with soft tissue impaction and impaction class A position 1 * Medical problem that may interfere with the procedures such as bleeding disorder & pregnant. * Uncooperative patient.

Design outcomes

Primary

MeasureTime frameDescription
Painimmediate post operative ,at three day pain change till fourteen day day .each patient well be asked to rate current and worst pain intensity on visual analogue scale (VAS ) of 0-10 with Zero being no pain and Ten corresponds to the worst pain(pain change during follow up period .

Secondary

MeasureTime frameDescription
evaluation of maximum inter incisal openingimmediate post operative ,at three day inter incisal change till fourteen day .assessment of MMO will be performed by measuring the distance in mm between the incisal edges of the upper and lower central incisor by using tape graduated method.

Contacts

Primary Contactalaaedein M abu al einain, master
surgeonalaamahmoud@gmail.com00201011618208
Backup ContactMamdouh S Sayed Ahmed, Professor
dr.mamdouhahmed@hotmail.com00201222173262

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026