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Effect of Temporization on the Peri-implant Soft Tissue of Immediate Implants: Randomized Controlled Clinical Trial

NCT03970811 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 22

Last updated 2022-01-10

No results posted yet for this study

Summary

This parallel arms, randomized controlled clinical trial will involve 22 systemically free patients with an unrestorable tooth in the upper esthetic zone. They will be randomly allocated to two equal groups. Group A (test group) will receive immediate implants with simultaneous immediate temporization, while group B (control group) will receive immediate implants with no temporization. After scaling root planing, the clinical parameters including PES, gingival recession, gingival thickness, postoperative pain and swelling as well as radiographic parameter obtained from Cone Beam Computed Tomography (CBCT) (buccal bone thickness) will be recorded. Immediate implant placement will be performed followed by simultaneous temporization in group A only. Postoperative medication will be prescribed to the patient and postoperative instructions will be explained in detail. Monthly follow-up will be performed to ensure performing proper oral hygiene. Data will be recorded at baseline (at time of implant insertion), three months, six months and nine months post prosthetic placement. Data collected will be tabulated and statistically analysed.

Conditions

  • Dental Restoration, Temporary

Interventions

PROCEDURE

Immediate Implants

dental implants are immediately placed after tooth extraction

PROCEDURE

temporary restoration

temporary restoration will be placed immediately after implant placement

PROCEDURE

final restoration

final restoration (loading) will be placed 3 months postsurgical

Sponsors & Collaborators

  • Zinedent

    collaborator UNKNOWN

  • Misr International University

    lead OTHER

Principal Investigators

  • Shahinaz G Elashiry, Assoc. Prof. · Periodontics Dep., Faculty of Dentistry, Misr International University

  • Hani El-Nahass, Assoc. Prof. · Periodontics Dep., Faculty of Dentistry, Cairo University

  • Fatma H Eldemerdash, Lecturer · Periodontics Dep., Faculty of Dentistry, Misr International University

  • Talaat Samhan, Lecturer · Fixed Prosthodontic Div., Faculty of Dentistry, Misr International University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2019-08-08
Primary Completion
2022-08-31
Completion
2022-12-22

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 NCT03970811 on ClinicalTrials.gov