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Effect of Immediate Placement and Loading of Compressive Versus Conventional Implants

NCT07601347 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2026-05-22

No results posted yet for this study

Summary

The current study aims to compare immediate placement and loading of compressive versus conventional dental implants after atraumatic extraction regarding the effectiveness, bone resorption and survival of each of them.

Conditions

  • Other Endosseous Dental Implant Failure

Interventions

PROCEDURE

Immediate implant placement and loading

1. Preoperative Cone beam 2. Articaine 4% local anesthesia in two sides 3. Piezoelectric device used around the badly decay tooth 4. Ensuring the preservation of the associated gingiva and papillae. 5. Following the elevation of the flap, atraumatic extraction by using piezoelectric device: A. The teeth will be retrieved without stress. B. The Conventional dental implant will be put directly into the alveolar bone c. Placement of healing abutment in conventional implant and measurement d. Stability measured using AnyCheck or periotest device of both implants and crestal bone level by periodontal probe postoperatively. e. Suturing f. Cone beam xray postoperatively g. Postoperative instructions and medications h. after one week immediate loading by placement of temporary pmma crown

PROCEDURE

Immediate implant placement and loading

1. Preoperative Cone beam 2. Articaine 4% local anesthesia in two sides 3. Piezoelectric device used around the badly decay tooth 4. Ensuring the preservation of the associated gingiva and papillae. 5. Following the elevation of the flap, atraumatic extraction by using piezoelectric device: A. The teeth will be retrieved without stress. B. The Compressive dental implant will be put directly into the alveolar bone c. Stability measured using AnyCheck or periotest device of both implants and crestal bone level by periodontal probe postoperatively. d. Suturing e. Cone beam xray postoperatively f. Postoperative instructions and medications g. after one week immediate loading by placement of temporary pmma crown

Sponsors & Collaborators

  • Ahmed Nagi Alghandour

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
CROSSOVER

Eligibility

Min Age
20 Years
Max Age
40 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2025-12-01
Primary Completion
2026-12-01
Completion
2026-12-01

Countries

  • Egypt

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07601347 on ClinicalTrials.gov