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Bone Height Changes In Three Implants Retained Mandibular Overdenture

K

Kafrelsheikh University

Status

Completed

Conditions

Implant Site Reaction
Bone Loss

Treatments

Other: locator attachment to retain mandibular over denture
Other: ball attachment to retain mandibular over denture
Other: telescopic attachment to retain mandibular over denture

Study type

Interventional

Funder types

Other

Identifiers

NCT04928274
KD/11/21

Details and patient eligibility

About

this study was to compare the bone height changes around three implant telescopic, locator, and ball retained mandibular overdentures. radiographic changes in peri-implant tissue in three groups were evaluated

Full description

Twenty-four completely edentulous patients were recruited from the outpatient clinic of Removable Prosthodontics Cairo University. All patients recruited were seeking to install implants in their lower jaw, and have to meet the following inclusion criteria: age ranging from 50 to 69 years old, patients should have no contra-indication for implant installation, all patients should perform a glycosylated hemoglobin analysis and only up to 8 were included in the study. All patients had to sign an informed consent before the start of the study, and have to comply with the assigned follow-ups. Patients with any contraindications for implant placement or those who didn't comply with the follow ups were excluded from the study.

All patients included had maxillary and mandibular complete dentures fabricated following the conventional steps, after a period of 6 weeks adaptation, all patients were ready for implant installation. The lower denture was duplicated into a radiographic stent, having radio-opaque markers in the areas of implant installation. All patients had a CBCT x ray wearing the radiographic stent, to allow for proper implant planning and to visualize the height and width of the osteotomy site. The radiographic stent was then modified to a surgical stent by making a tunnel corresponding to the site of implant installation. All Patients in this study received three implants in the lower jaw at the premolar-canine area bilaterally and one implant in the midline at the central incisor area.

Enrollment

24 patients

Sex

All

Ages

50 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • age ranging from 50 to 69 years old, patients should have no contra-indication for implant installation, all patients should perform a glycosylated hemoglobin analysis and only up to 8 were included in the study

Exclusion criteria

  • Patients with any contraindications for implant placement or those who didn't comply with the follow ups were excluded from the study.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

24 participants in 3 patient groups

ball retained mandibular over denture
Other group
Description:
each patient in this group received 3 implant installed in mandible and 3 ball attachments for retention of over denture
Treatment:
Other: ball attachment to retain mandibular over denture
locator retained mandibular over denture
Other group
Treatment:
Other: locator attachment to retain mandibular over denture
telescopic retained mandibular over denture
Other group
Treatment:
Other: telescopic attachment to retain mandibular over denture

Trial contacts and locations

3

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Data sourced from clinicaltrials.gov

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