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Digital Obturators in Maxillectomy Cases

T

Tanta University

Status

Completed

Conditions

Device Malfunction

Treatments

Device: obturator

Study type

Interventional

Funder types

Other

Identifiers

NCT06527053
RP08-21\4

Details and patient eligibility

About

Using Digital approach to treat patients with maxillofacial defects without surgical intervention

Full description

Evaluating digital dental and maxillofacial obturators to artifitially close maxillofacial defects in paients with oral cancer and patients with mucormycosis fungal post covid infection.

Craeting Digitized database for all patients included in the study.

Recording casses with post covid infection in specific period.

Enrollment

7 patients

Sex

All

Ages

20 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

All participants in this study will be selected according to the following criteria:

  • Patients with maxillary defects Class I and class II Aramany Classification with completely healed tissues.
  • Patients' age ranging from 20 to 70 years old.
  • Nearly intact mandibular arch.

Exclusion criteria

Participants with the following criteria will be excluded from the study:

  • Physical or mental instability.
  • Completely edentulous patients.
  • Patients presenting allergy to materials being used.
  • Patients lacking compliance to maintain acceptable oral hygiene.
  • Patients taking radiotherapy

Trial design

Primary purpose

Device Feasibility

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

7 participants in 2 patient groups

digital obturator
Experimental group
Description:
new approach to create device
Treatment:
Device: obturator
conventional obturator
Experimental group
Description:
old approach to create device
Treatment:
Device: obturator

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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