Not yet recruitingNCT06628492Updated Oct 8, 2024

Surgical Guided Fabricated From Two Different Printing Materials

An interventional study of stainless steel printed surgical guide and resin printed surgical guide in Partial-edentulism, sponsored by Suez Canal University. Not yet recruiting. Open to participants aged 21 Years and older. Per ClinicalTrials.gov, last updated 2024-10-08.

Sponsored by Suez Canal University · Not applicable, Interventional, and Treatment

From the registry’s dates

Primary completion was expected by Nov 2024, 1 year 11 months ago, but the record still lists the study as not yet recruiting.

Phase: Not applicable
Study type: Interventional
Enrollment: 12
Allocation: Non-randomized
Ages: 21 Years and older
Sex: All

Study summary

implant will be inserted in patients with kennedy class 3 or 4 partially edentulous mandible .the implants will be inserted using teeth supported surgical guide fabricated from two different materials

Conditions studied

Partial-edentulism

In context

Lead sponsor

Suez Canal University is the lead sponsor of 157 studies on the registry; 37 are open to participants now.

Counted across the registry records on this site, refreshed daily.

Who can participate

Ages eligible: 21 Years and older
Sexes eligible: All
Accepts healthy volunteers: No

Inclusion criteria

Patients with skeletal Angle´s class I maxilla-mandibular relationship,
adequate inter-arch distance, have Kennedy class 3 or 4 partially edentulous mandible of more than 2 teeth missed and will be applied for the treatment of tooth loss and requiring fixed prosthodontic rehabilitation
normal Physical and psychological status to tolerate conventional implant procedures,
Their residual ridge had sufficient bone volume for implant installation and was covered by firm mucoperiosteum.

Exclusion criteria

Exclusion Criteria:

Smokers.
Patients undergoing chemotherapy or radiotherapy and immunocompromised patients.
Patients with, systemic disease that might complicate post-operative healing or contribute to bone resorption, e.g uncontrolled diabetes, psychological disorders, or alcohol, tobacco, or drug abuse
parafunctional habits, poor oral hygiene, limited mouth opening, severe alveolar bone deficiencies,

Study design

Phase: Not applicable
Primary purpose: Treatment
Allocation: Non-randomized
Intervention model: Single group
Masking: Double (Investigator, Outcomes assessor)
Enrollment: 12 participants (estimated)

Study arms

Experimental
group A implant inserted by stainless steel surgical guide
Device: stainless steel printed surgical guide
Active comparator
group B implant inserted by resin surgical guide
Device: resin printed surgical guide

Interventions

Devicestainless steel printed surgical guide
the patient will wear the stainless steel surgical guide for the insertion of one implant
Deviceresin printed surgical guide
the patient will wear the resin surgical guide for insertion of adjacent another implant implant

What researchers measure

Primary outcomes

linear deviation of inserted implant
coronal and apical deviation of inserted implant from virtually planned one in millimeter.
Time frame: 1 month
angular deviation of inserted implant
angular deviation of inserted implant from virtually planned one in angles.
Time frame: 1 month

Study locations

No study locations are listed for this record.

Updates

Tracking since Sep 25, 2026

No changes since tracking began. The registry record was last updated on Oct 8, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗

Registry details

Key details

Study ID: NCT06628492
Lead sponsor: Suez Canal University
Responsible party: Sponsor
First posted: Oct 8, 2024
Start date: Oct 2024 (estimated)
Primary completion: Nov 2024 (estimated)
Completion: Nov 2024 (estimated)
Last update: Oct 8, 2024

Study contacts

ahmed m hebeshi, Phd

Contact

ahmed_hebeshi@dent.auez.edu.eg

00201282531256

Oversight

FDA-regulated drug: No
FDA-regulated device: No

View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Oct 2024. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Other studies from this sponsor

Suez Canal University

Start the discussion