Single vs. Two Implants for Mandibular Overdentures

Not Applicable

Completed

• Conditions: Bleeding on Probing; Alveolar Bone Loss; Mastication; Dental Plaque; Periodontal Index
• Interventions: Device: Root form dental implant

• Registration Number: NCT06599450
• Lead Sponsor: Al-Azhar University

Brief Summary

This study aimed to compare the use of single implants in the symphyseal and parasymphyseal, and two implants were inserted in the canine area bilaterally to assist mandibular complete overdentures regarding clinical evaluation, marginal bone loss, and masticatory efficiency. The null hypothesis was that there was no statistically significant difference in clinical evaluation, marginal bone loss, and masticatory efficiency among single symphyseal implants, single parasymphyseal implants, and two-implant-assisted complete mandibular overdentures.

Detailed Description

This randomized, controlled clinical trial compared the symphyseal and parasymphyseal single implants versus two implants in complete mandibular overdentures. Fifteen completely edentulous male patients (50-65 years) were chosen and randomly grouped into three equal groups (five patients in each) according to the position and number of the received implants to assist mandibular complete overdentures. Group I: single median implant. Group II: single parasymphyseal implant. Group III: two implants were inserted in the canine area bilaterally. After three months of osseointegration, the lower denture was transformed into an implant-assisted complete mandibular overdenture. Clinical observations were documented on the day of loading, three, six, and nine months later for each implant. Follow-up CBCT scans were performed to assess marginal bone loss on the day of loading, six and twelve months later. The masticatory efficiency evaluation was conducted one month and three months after loading.

Study Timeline

• Study Start: 2021-10-01
• Primary Completion: 2023-11-01
• Study Completion: 2024-01-01
• Status Verified: 2024-09
• Study First Submitted: 2024-09-12
• Study First Submitted QC: 2024-09-13
• Last Update Submitted: 2024-09-13
• Study First Posted: 2024-09-19
• Last Update Posted: 2024-09-19

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Male
• Target Recruitment: 15

Inclusion Criteria

• patients with a class I Maxillo-mandibular jaw relationship
• patients with residual ridges had normal morphology, were free from severe bony undercuts or flabby tissue, and were covered by firm mucoperiosteum.
• A cone beam CT of the lower arch was made to detect the presence of pathological lesions, remaining roots, or impacted teeth in the arch and evaluate both bone quality and quantity, especially in the area of interest

Exclusion Criteria

• patients with current chemotherapy or radiotherapy, bleeding disorders, uncontrolled diabetes
• patients with a history of drug therapy that interferes with bone resorption or deposition (e.g., the prolonged use of glucocorticoids, antiresorptive medications, selective serotonin reuptake inhibitors, and proton-pump inhibitors),
• Those with any physical reasons that could affect follow-up, psychiatric problems, heavy smokers, drug or alcohol addicts, immunocompromised patients, abnormal jaw relationship, inadequate inter arch space.
• patients with temporomandibular disorders and para-functional habits (e.g., bruxing and clenching).

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
One median implant	Root form dental implant	One median implant to retain mandibular complete overdenture
One parasymphyseal implant	Root form dental implant	One parasymphyseal implant to retain mandibular complete overdenture
Two implants	Root form dental implant	Two implants in the intraforaminal distance to retain mandibular complete overdenture

Primary Outcome Measures

Name	Time	Method
Change in the plaque index	The plaque index was documented at follow-up visits on the day of loading, three, six, and nine months later for each implant.	The presence and amount of plaque were determined at the four sites around the implant (mesial, distal, buccal, and lingual) and scored from zero to three. Grade 0: No plaque by probing. Grade 1: film of plaque detected by probing. Grade 2: Visible plaque with the naked eye. Grade 3: abundant soft material in the sulcus, mucosal margin, and adjacent implant surface.
Change in the pocket depth	The pocket depth was documented at follow-up visits on the day of loading, three, six, and nine months later for each implant.	The pocket depth was measured by inserting a graduated plastic periodontal probe between the oral sulcular epithelium and the implant with minimal pressure at the midpoint of the four surfaces. The distance from the bottom of the sulcus to the mucosal margin was measured and recorded to the nearest millimeter; the mean of four readings was considered the pocket depth for this group at the chosen time
Change in the bleeding index	The bleeding index was documented at follow-up visits on the day of loading, three, six, and nine months later for each implant.	The bleeding index was assessed for the four surfaces while measuring the pocket depth if the bleeding was visible after probing within 20 seconds. It is typically scored as 0 (no bleeding), 1 (bleeding point), 2 (single line of blood), or 3 (heavy or profuse bleeding). The mean of four readings was considered the bleeding index for this group at the chosen time
Change in bone level around implant	Immediately after loading, six months, and twelve months later	Calculating average bone height involves dividing the sum of buccal, lingual, mesial, and distal bone height by 4. The real bone loss can be calculated by subtraction from the implant length
Change in the masticatory efficiency	The masticatory efficiency was documented at follow-up visits one month and three months after the overdenture insertion	The masticatory efficiency was assessed when the patient ate three different types of food (carrot, apple, and banana) with varying degrees of hardness, cut into standardized pieces (1 cm cube each). The collected data included the following measurements: the chewing stroke count before the first swallow, the chewing stroke count until the oral cavity is empty of food, the count of swallows until the oral cavity is empty of food, the time estimated in seconds until the first swallow, and the time estimated in seconds until the oral cavity is empty of food.

Trial Locations

Locations (1)

Faculty of Dental Medicine, Al-Azhar University, Assuit; 🇪🇬 Assuit, Egypt