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Dental ImplantNCT06910007

Accuracy of Various Advanced Treatment Planning Software for Static Computer Guided Surgery in Dental Implant

A study testing dental implant will be inserted using surgical guide and dental implant in people with Dental Implant, run by University of Baghdad.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Official record
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Trial summary

This study will be conducted to investigate the accuracy of Blue sky plan bio , exoplan ,and real guide advanced treatment planning software required for static computer guided surgery designing and manufacturing. Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
Conditions the study is for
Dental Implant
What is being tested?
dental implant will be inserted using surgical guide and dental implant
Type of treatment
Surgery or procedure
Could I receive a placebo?
No, everyone receives an active treatment
How many people
60 participants
Where
No sites listed yet
Study dates
20 Apr 2025to Dec 2026
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • partially edentulous adults with at least three teeth remaining.
  • an expected sufficient bone volume to perform implant insertion with at least a 3.5mm Cybermed dental implant without simultaneous bone augmentation.
  • extractions performed at least 3 months earlier.
  • potential earlier sinus grafting was performed at least 6 months prior to implant placement.
  • Patients with absence of any periodontal problems in the adjacent teeth.
  • 7- stable medical condition to undergo implant surgery (ASA 1 or 2).

Who cannot join

  • Physical or psychological disorders generally prohibiting implant therapy. After initial screening.
  • Patients with a history of bruxism
  • Patients with over eruption of the opposing tooth.

About this study

Official title: Accuracy of Advanced Treatment Planning Software for Static Computer Guided Surgery ( Blue Sky Plan Bio, Exoplan, Real Guide Computer Software)

This study will be conducted to investigate the accuracy of Blue sky plan bio , exoplan ,and real guide advanced treatment planning software required for static computer guided surgery designing and manufacturing.

Conditions
Dental Implant
Being tested
dental implant will be inserted using surgical guide, dental implant

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • dental implant will be inserted using surgical guideProcedure or surgery

    dental implant will be inserted using blue sky plan computer software

  • dental implantProcedure or surgery

    surgical guide will be fabricated using exoplan computer software

  • dental implant will be inserted using surgical guideProcedure or surgery

    surgical guide will be fabricated using real guide computer software

Study groups in NCT06910007
Study groupRoleWhat they receive
blue sky plan groupActive comparatorsurgical guide will be fabricated using Blue sky plan computer software
Receives: Procedure: dental implant will be inserted using surgical guide; Procedure: dental implant
exoplan groupActive comparatorsurgical guide will be fabricated using Exoplan computer software
Receives: Procedure: dental implant will be inserted using surgical guide; Procedure: dental implant
Real guide groupActive comparatorsurgical guide will be fabricated using Real guide computer software
Receives: Procedure: dental implant will be inserted using surgical guide; Procedure: dental implant

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. deviation between planned and actual implant position when using different planning software

    measurement will be done by superimposition two CBCTs showing the pre-operation ( planned) and post operation implant position which will reveal the deviation in millimeter in regards to entry point ,apical ,and angular deviation of dental implant using specified tool within the planning software

    Measured: 14 days

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted4 Apr 2025
  2. Study start20 Apr 2025 (estimated)
  3. Primary completion28 Nov 2026 (estimated)
  4. Study completionDec 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Crossover
Masking
Single blind
Who is masked
Participant
Enrolment
60 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06910007
Sponsor's protocol ID
1025 in 11-2-2025
Status last verified
Apr 2025
First submitted
22 Mar 2025
Last updated
4 Apr 2025
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing dental implant will be inserted using surgical guide and dental implant in people with Dental Implant, run by University of Baghdad.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 6 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 4 Apr 2025. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

deviation between planned and actual implant position when using different planning software (time frame: 14 days). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 4 Apr 2025.

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Clinical Trial NCT06910007 | AzTrials