A Study Comparing Two Different denture base materials in implant retained overdentures

Clinical and Microbial Evaluation of Two Different Implant Retained Mandibular Overdentures (Randomized Clinical Trial)

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

PACTR

Registry ID

PACTR202511688761752

Enrollment

Registered

2025-11-20

Start date

2024-05-01

Completion date

Unknown

Last updated

2026-09-14

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

Conditions

None listed

Interventions

mandibular complete dentures processed into heat cured acrylic resin

mandibular thermoplastic nylon denture

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Edentulous patients were chosen between the ages of 60 to 70 years old All patients’ ridges were covered with firm mucosa, free from any signs of inflammation or ulceration, exhibit adequate height and width of the residual alveolar ridge have sufficient inter arch space. Patients were free from any metabolic or bone disorder that contraindicate implant installation.

Exclusion criteria

Exclusion criteria: Patients with oral or systemic diseases patients with xerostomia or excessive salivation. Patients with parafunctional habits (bruxism or clenching) or history of temporo-mandibular dysfunction or brain disorders or psychiatric disorders.

Design outcomes

Primary

Measure	Time frame
Clinical (Periodontal) evaluation, Pocket depth (Depth of gingival sulcus) Plaque index	—

Secondary

Measure	Time frame
Denture swabs and isolation of Candida albicans;Measurement of satisfaction and Oral Health–Related Quality of Life (OHRQoL)	—

Countries

Egypt

Contacts

Public ContactNoha Alloush

lecturer

yunie0959@gmail.com+201112295457

Outcome results