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Immediate Versus Delayed Loading for Implants Retaining Mandibular Complete Overdenture

Immediate Versus Delayed Loading for Immediately Inserted Implants Retaining Mandibular Complete Overdenture

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05620797
Enrollment
14
Registered
2022-11-17
Start date
2018-03-01
Completion date
2021-06-30
Last updated
2022-12-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bone Loss, Dental Implant

Brief summary

The aim of this study will be to compare the amount of marginal bone height changes between immediate and delayed loading for immediately inserted implants used as abutments of mandibular overdenture.

Interventions

OTHERImmediate loading of the implants

Patients of this group will be rehabilitated by implant-retained mandibular overdenture with immediate loading of the implants as opposed to conventional maxillary complete dentures.

OTHERDelayed loading of the implant

Patients of this group will be rehabilitated by implant retained mandibular overdenture with delayed loading of the implants (after 3 months) opposed by conventional maxillary complete dentures

Sponsors

Hams Hamed Abdelrahman
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
55 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Patient having two standing mandibular canines with compromised prognosis (which indicted for extraction, without any preapical lesions nor acute infection) and have an adequate labial bone thickness. * Patient having opposing completely edenteolous maxilla. * Patients having normal maxilla-mandibular relationship and sufficient inter arch distance was insured by through tentative jaw relation record. * Patients with good oral hygiene. * Enough bone volume for implants in the interforaminal region (adequate bone quality and quantity)

Exclusion criteria

* Mental disorder patients who are not capable of making a decision or narcotic drug addicts. * Patients with Tempro-Mandibular Joint disorders * Patients undergoing radiotherapy or chemotherapy * Patients with systemic diseases affecting bone metabolism * Uncooperative patients who have no understanding of the need of a regular follow-up. * Patient with pathological defects in the areas of implant insertion. * Vulnerable group as prisoners, mentally retarded patients.

Design outcomes

Primary

MeasureTime frameDescription
Change in bone lossat 3 months, 6 months, 9 months, 12 monthsEvery 3 months all patients were recalled for assessment of marginal bone loss. The assessment was done using digital periapical radiograph Ezsensor (Vatech intraoral radiographic sensor, Vatech, South Korea) and the technique of radiograph was paralleling technique using sensor holder (TROLLBYTE PLUS, TROLLDENTAL, UK) to ensure same position of cone through subsequent follow-up exposures

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026