Skip to content

Retention of Three Different Types of Telescopic Attachments

Retention of Three Different Secondary Copings in Telescopic Attchments Used to Stabilize Implant Retained Mandibular Overdenture a Randomized Clinical Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06632548
Acronym
Overdenture
Enrollment
30
Registered
2024-10-09
Start date
2022-08-30
Completion date
2024-03-30
Last updated
2024-10-09

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

Conditions

Denture Retention, Edentulism

Keywords

overdenture-telescopic attachment-poly ether ketoneketone-PEKK-, milled titanium, 3d printed cobalt chromium, implant retained overdenture, mandibular overdenture

Brief summary

This study was conducted on thirty patients. These patients were divided into three groups in a random manner to compare the retention forces between three different types of secondary crowns used to stabilize two implant mandibular overdentures. in all groups the primary coping was fabricated from milled titanium while the secondary coping was milled titanium in first group ,3D printed cobalt chromium in the second group and milled poly ether ketone ketone in the third group the retention forces was measured using forcemeter immediately after insertion and after 3,6, months

Detailed description

A thirty edentulous patients Was selected from outpatient clinic of Exclusion criteria: 1. systemic and metabolic disorders that may complicate osseointegration. 2. Patients receiving bisphosphonates. 3. patients receiving radiotherapy. The patients was assigned into three groups using balanced randomly. Patients was randomly allocated into one of three groups using random numbers generated using Excel program. Group I included patients who received 2 implants and telescopic overdentures with milled titanium primary and secondary coping Group II included patients who received telescopic overdentures with milled titanium primary coping and three dimensionally printed secondary coping GroupIII patients recived milled titanium primary coping and poly ether ketone ketone secondary copings (PEKK) secondary coping All patients signed an informed consent. Surgical and prosthetic protocols: A radiographic stent with gutta percha markers at the canine region was fabricated and the patient was instructed to wear it during cone beam radiographic evaluation to evaluate proposed implant sites regarding bone height and thickness, and approximation to vital structures (mental foramen). Radiographic template was converted to surgical template. The two implants was inserted nearly parallel as possible. If inclination of the implants was inevitable buccally or lingually due to mandibular concavities, the inclination was compensated later during design of primary copings. The implants was inserted in the canine region with two steps surgical protocol. After three months of the insertion and osseointegration implants was exposed and healing abutments was inserted after gingival healing implant level impression will be taken. The metallic primary coping was milled with 2-degree convergence for all cases while the second coping was milled titanium or 3D printed cobalt chromium or milled PEKK according the patient group. the primary copings was screwed to the implants and the secondary coping pick up was done and patient was instructed to follow oral hygiene measures and was scheduled for periodic follow up every 3 months. Evaluation of overdenture retention: Force meter device was used to measure the retention of the mandibular overdenture in Newton. The patient was seated on upright position and asked to open his mouth until the occlusal surface of the lower denture is parallel to the floor and the maximum dislodging force to remove the denture is recorded using digital forcemeter. Measurement of retention forces was made immediately after overdenture insertion and repeated at 3,6,9and 12 months after insertion after by independent dental personnel blinded to treatment groups.

Interventions

two implant retained mandibular overdenture with telescopic attachment

Sponsors

Moatz Aly Ahmed Hussien
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
55 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

1. un-satisfaction with the retention of mandibular dentures due to mandibular ridge atrophy and desired to have more stable prosthesis, 2. sufficient remaining bone in height, width and thickness in the interforaminal area to allow installation of at least 3.5mm diameter implants. 3. Adequate amount of interarch space of at least 12mm from the occlusal plane of the mandibular denture to the mucosa of the ridge. Patients with the 4- age range 55 to 75 years. \-

Exclusion criteria

1\) systemic and metabolic disorders that may complicate osseointegration. 2) Patients receiving bisphosphonates. 3) patients receiving radiotherapy. \-

Design outcomes

Primary

MeasureTime frameDescription
retention forcesfrom insertion time up to one year follow upretention forces of three different type secondary coping telescopic attachments used to stabilize two implant mandibular overdenture these attachments are made of either milled titanium, 3D printed cobalt chromium or milled poly ether ketone ketone

Countries

Egypt

Outcome results

None listed

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