Viewing Study NCT05289752



Ignite Creation Date: 2024-05-06 @ 5:22 PM
Last Modification Date: 2024-10-26 @ 2:28 PM
Study NCT ID: NCT05289752
Status: COMPLETED
Last Update Posted: 2023-04-20
First Post: 2022-02-27

Brief Title: Direct Versus Indirect Pick up of the Locator Retentive CapsWithin-patient Study
Sponsor: Mansoura University
Organization: Mansoura University

Study Overview

Official Title: Direct Versus Indirect Pick up of the Locator Retentive Caps for Two Implant-retained Mandibular Overdenture Calibration of the Manufacturer Retentive Force and the Clinical Retention Within-patient Study
Status: COMPLETED
Status Verified Date: 2023-02
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The purpose of this study will be to evaluate the effect of direct and indirect pick up of the locator retentive caps and compare the clinical results with those of the manufacturer retentive force
Detailed Description: Patient selection

For this study 30 patients were selected from the clinic of Prosthodontic Department Faculty of Dentistry Mansoura University

According to pick up technique for the locator retentive caps the overdentures will be classified into two groups as follows Group1 The retentive caps will be picked up by indirect method on the cast then by the direct method Group2 The retentive caps will be picked up in the patient by the direct method first then by the indirect method

For both groups the clinical retention will be measured after using pink and blue retentive inserts respectively

All implants were inserted using computer-guided implant surgery and conventional loading protocol was used

Evaluation methods The clinical retention of each insert will be calibrated as regards the manufacturers value

Also the laboratory retention will be assessed for the two groups and calibrated as regards the manufacturers value

Measurements will be done immediately three and six months after each overdenture insertion

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None