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Passive Fit of CAD/CAM Screw-retained Metal Frameworks Versus Screwmented Ones

Cairo University (CU) logo

Cairo University (CU)

Status

Unknown

Conditions

Jaw
Edentulous

Treatments

Procedure: Digitally constructed frameworks after implant placement
Procedure: Digitally constructed frameworks before implant placement

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

CAD/CAM (computer aided design/ computer aided manufacturing) constructed screw retained implant supported frameworks give solutions for the problems arising from the lost wax technique by improving accuracy, adaptation and passive fit of the final restoration. However, concerns about the passive fit of a pre-implant insertion CAD/CAM constructed framework still exists due to the expected errors in imaging, registration, surgical guide construction, adaptation and hence transferring the planned position intra-orally.

Full description

  1. PICO Format: Population: mandibular free end saddle requiring 2 implants. Intervention: Digitally fabricated screw-mented retained metal frameworks constructed before implant placement Control: Digitally fabricated screw retained metal frameworks constructed after implant placement

Outcome:

Outcome Measuring device Measuring unit Passive fit One screw test Binary 13 Screw resistance Binary Radiographic ( digital periapical radiography) Binary III. Methods A) Participants, interventions & outcomes 9. Study settings: i. The study will be conducted at Department of Oral Implantology, faculty of oral and dental medicine, Cairo University, Egypt. ii. Participants will be selected from the outpatient clinic of implantology department, faculty of oral and dental medicine, Cairo University, Egypt. 10. Eligibility criteria: A-Inclusion criteria: i- Mandibular Kenndy Class I. ii- Opposing completely dentulous, fully or partially restored dentition. iii- Good oral hygiene. iv- The patient should have bone for implants, minimum bone height 10 mm and minimum bone diameter should be 6 mm. v- Adequate inter arch space for restoration 15mm or more. vi- Adult patients age ≥18 years B- Exclusion criteria: i. any medical disorder that could complicate surgical phase or affect osteointegration. Radiation chemotherapy. ii. smokers more than 10/daily. iii. Uncooperative patients. iv. Patients with Para-functional habits v. Patients with severe periodontal diseases. vi. Patients with limited mouth opening. vii. Presence of intraoral pathological lesions. viii. Diabetic (HbA1c >7.5%).

Enrollment

8 estimated patients

Sex

All

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

.Inclusion Criteria:

  • Mandibular Kenndy Class I.
  • Opposing completely dentulous, fully or partially restored dentition.
  • Good oral hygiene.
  • The patient should have bone for implants, minimum bone height 10 mm and minimum bone diameter should be 6 mm.
  • Adequate inter arch space for restoration 15 mm or more.
  • Adult patients age ≥18 years

Exclusion Criteria:

    • . any medical disorder that could complicate surgical phase or affect osteointegration. Radiation chemotherapy.
  • ii. smokers more than 10/daily.
  • iii. Uncooperative patients.
  • iv. Patients with Para-functional habits
  • v. Patients with severe periodontal diseases.
  • vi. Patients with limited mouth opening.
  • vii. Presence of intraoral pathological lesions.
  • viii. Diabetic (HbA1c >7.5%)

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

8 participants in 2 patient groups

digitally constructed frameworks before implant placement
Experimental group
Description:
Intervention group in which the edentulous area will be restored with 3-implant screwmented CAD/CAM frameworks constructed based on planned implant positions.
Treatment:
Procedure: Digitally constructed frameworks before implant placement
digitally constructed frameworks after implant placement
Active Comparator group
Description:
Control group: edentulous area will be restored with 3-implant conventional screw retained CAD/CAM frameworks constructed after implant placement
Treatment:
Procedure: Digitally constructed frameworks after implant placement

Trial contacts and locations

1

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Central trial contact

mohamed Elsayyed, BDS; Iman Radi, PhD

Data sourced from clinicaltrials.gov

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