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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05101941
Other study ID # Immediate implants_2020
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date December 8, 2020
Est. completion date October 7, 2021

Study information

Verified date October 2021
Source Alexandria University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Compromised teeth with periapical pathologies are removed before dental implant placement and sockets are left to heal. Some clinicians began to immediately place dental implants in fresh extraction sockets associated with chronic inflammatory periapical lesions and these studies revealed high success rates


Description:

12 implants will be immediately placed in sockets associated with chronic periapical granuloma. Clinical (Wound healing, Pain, swelling, implant stability) and radiographic parameters (Peri-implant radiolucency) will be evaluated


Recruitment information / eligibility

Status Completed
Enrollment 12
Est. completion date October 7, 2021
Est. primary completion date October 7, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria: - Adult patients ranging from 18 to 45 years with no gender predilection agreed to come for minimum follow-up visits for 6 months. - Adequate bone beyond teeth apices without jeopardizing any anatomical structure. - Single rooted mandibular teeth with chronic inflammatory periapical lesions represented as periapical radiolucency, pulp necrosis, sinus tract, failed RCT. Exclusion Criteria: - Smokers and alcoholics. - Medically compromised patients having uncontrolled diabetes or coagulation disorders. - Restorable teeth. - Periodontitis.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Immediate dental implants
Implants will be immediately placed in sockets associated with chronic periapical granuloma Extraction of non-restorable Teeth with periapical granuloma and socket debridement will be done then implants will be placed

Locations

Country Name City State
Egypt Alexandria Faculty of Dentistry Alexandria

Sponsors (1)

Lead Sponsor Collaborator
Hams Hamed Abdelrahman

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in Implant stability It will be measured by implant stability meter (Osstellâ„¢) immediately, at 3 months and 6 months
Primary Change in peri implant radiolucency Immediate post-operative and after 6 months CBCT will be requested in order to compare the dimension of the periapical lesion in millimeters using OnDemand system. immediately, and 6 months
Secondary Change in pain score It will be recorded daily for the first week through a 10-point Visual Analogue Scale (VAS) from 0 to 10 (0-1= None, 2-4= Mild, 5-7= Moderate, 8-10= Severe). within a week
Secondary Change in swelling status It will be recorded daily for the first week through a 10-point scale with 4 parameters will be used.
none (no swelling), light (intraoral, localized to the treated area), moderate (extraoral swelling localized to the treated area), and severe (extraoral swelling extending beyond the treated area)
within a week
Secondary Change in Early Wound Healing Index Using Early Wound Healing Index (EHI), it will be evaluated across weeks 2, 4 and 8.
(EHI; 1: complete flap closure-no fibrin line; 2: complete flap closure-fine fibrin line; 3: complete flap closure-fibrin clot; 4: incomplete flap closure-partial necrosis; 5: incomplete flap closure-complete necrosis).
at 2 weeks, 4 weeks, and 8 weeks
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