Modified Pedicle Subepithelial Connective Tissue Graft for Interdental Papillary Reconstruction Around Delayed Implants in the Esthetic Zone: A Case Series Trail

Papilla Reconstruction Clinical Trial

— delay implant  

Official title:

تعديل النسيج الضام عنيق تحت الظهارة من أجل إعادة بناء حليمي بين الأسنان حول الزراعه المتأخره في المنطقة الجمالية

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04843826
• Other study ID #: PER 111
• Secondary ID: per 122
• Status: Recruiting
• Phase: N/A
• Start date: April 14, 2020
• Est. completion date: September 14, 2021

Study information

• Verified date: April 2020
• Source: Cairo University
• Contact: Ahmed Sadek Mohamed, master
• Phone: 23634965
• Email: ahmed.sadek[@]dentistry.edu.cu.eg
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This case series trial aims to evaluate the effect of a modified pedicle subepithelial connective tissue graft in creating anatomical papilla around one-stage delayed implant in the esthetic zone to establish better esthetics.

Description:

• Preparation of the implant site will be prepared by a crestal incision on the ridge bisecting the existing keratinized mucosa and vertical releasing incisions extending to the vestibule. The papillae of the adjacent teeth are not included in the flap design.

• A full thickness flap will be raised buccally exposing the underlined ridge of the implant site. A surgical drill guide will be used for the precise placement of the pilot drill. After pilot drill application, the osteotomy will be prepared with the corresponding size of parallel drill.

• The implant will be placed in the recipient site by means of an insertion device. The implant neck will be positioned flushing with the crestal bone level.

• The healing abutment extension of the implant will be placed in such a way that the head of the implant protruded about 2 to 3 mm from the bone crest.

• Reassessment of the case to assure absence of any signs of inflammation and presence of normal tissues before the surgical procedure

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 10
• Est. completion date: September 14, 2021
• Est. primary completion date: May 20, 2020
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: N/A and older

Eligibility

Exclusion Criteria:

1. Pregnant females.

2. Smokers as smoking is a contraindication for any plastic periodontal surgery (Khuller, et al., 2009)

3. Handicapped and mentally retarded patients.

4. Patients undergoing radiotherapy.

5. Presence of systemic disease that would affect wound healing

Related Conditions & MeSH terms

• Papilla Reconstruction

Intervention

Procedure:
• papilla reconstruction
subepithelial connective tissue graft for interdental papillary reconstruction around delayed

Locations

Country	Name	City	State
Egypt	Cairo University Faculty of Dentistry	Cairo	Manial

Sponsors (1)

Lead Sponsor	Collaborator
Ahmed Sadek Mohamed

Country where clinical trial is conducted

Egypt, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	papilla height	Periodontal probe and reference line	3 month