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

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

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04843826
Acronym
delay implant
Enrollment
10
Registered
2021-04-14
Start date
2020-04-14
Completion date
2021-09-14
Last updated
2021-04-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Papilla Reconstruction

Brief 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.

Detailed 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

Interventions

PROCEDUREpapilla reconstruction

subepithelial connective tissue graft for interdental papillary reconstruction around delayed

Sponsors

Ahmed Sadek Mohamed
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Case Series trial

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
papilla height3 monthPeriodontal probe and reference line

Countries

Egypt

Contacts

Primary ContactAhmed Sadek Mohamed, master
ahmed.sadek@dentistry.edu.cu.eg23634965
Backup Contactweam Ahmed el batawy, PHD
weamelbatawy@dentistry.edu.cu.eg23634965

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026