NCT07846384

Brief Summary

After tooth extraction the alveolar ridge undergoes an unescapable physiological phase of remodeling. The major changes occur during the first three months of healing with a reduction in the dimension of the socket of about 11%-22% vertical bone loss and 29%-63% horizontal bone loss. Such dimensional change will compromise prosthetic replacement in the future, so we make alveolar ridge preservation in order to future complications

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
28

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Apr 2025

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

April 25, 2025

Completed
1.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 1, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2026

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

September 23, 2026

Completed
6 days until next milestone

First Posted

Study publicly available on registry

September 29, 2026

Completed
Last Updated

September 29, 2026

Status Verified

November 1, 2024

Enrollment Period

1.3 years

First QC Date

September 23, 2026

Last Update Submit

September 23, 2026

Conditions

Outcome Measures

Primary Outcomes (2)

  • volumetric bone change after socket preservation, and it will be measured by CBCT.

    CBCT will be taken 3 times: first at the baseline before extraction, second during the follow-up period after 3 months, and third after 6 months.

  • Change in Alveolar Bone Volume After Socket Preservation Measured by CBCT

    volumetric bone change after socket preservation, and it will be measured by CBCT. Soft tissue change is measured by a periodontal probe. Soft tissue thickness will be measured using an intraoral scanner. pain by VAS score.

    3 months and 6 months

Study Arms (2)

sticky bone group

ACTIVE COMPARATOR

socket preservation using sticky bone (Xenograft + I-PRF) after tooth extraction to avoid future complications and dimensional change following tooth extraction with a bicompatible material with previous studies on the efficacy of the material in alveolar ridge preservation.

Combination Product: sticky dentin groupCombination Product: sticky bone

sticky dentin group

EXPERIMENTAL

socket preservation using sticky dentin (demineralized dentin + I-PRF)

Combination Product: sticky dentin groupCombination Product: sticky bone

Interventions

sticky dentin groupCOMBINATION_PRODUCT

The autogenous demineralized dentin is used in socket preservation. as it shares a similar composition to the bone. Demineralized dentin is an osteoinductive and osteoconductive material, making it an alternative to xenograft in socket preservation. The addition of the PRF helps in healing and pain reduction. Xenograft is an osteoconductive material, and a previous study showed a reduction in dimensional change following tooth extraction. The effect of the sticky dentin on the bone and soft tissue is measured using the CBCT, intraoral scanner, and periodontal probe.

Also known as: sticky tooth
sticky bone groupsticky dentin group
sticky boneCOMBINATION_PRODUCT

Socket preservation using sticky dentin (Xenograft + I-PRF) after tooth extraction.

sticky bone groupsticky dentin group

Eligibility Criteria

Age20 Years - 55 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • patient (20-55) years old
  • non-smoker
  • medically free
  • non-restorable tooth.
  • anterior zone
  • Type 1 extraction socket

You may not qualify if:

  • medically compromised patient (uncontrolled diabetes, hyperthyroidism).
  • pregnant female.
  • history of chemo or radiotherapy

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Faculty of Dentistry, October University for Modern Sciences and Arts (MSA University)

Giza, 02, Egypt

Location

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, INVESTIGATOR
Purpose
PREVENTION
Intervention Model
PARALLEL
Model Details: Research focuses on autogenous demineralized dentin bone in order to overcome problems with the autograft or allograft or synthetic bone. Bone and teeth are very similar in their composition, as both are composed of inorganic substances such as hydroxyapatite and calcium phosphate and organic substances like collagen, as dentin is composed of 65% inorganic and 35% organic substances such as collagen type 1 , growth factors such as bone morphogenic protein, as the perivascular mesenchymal stem cells will differentiate into cartilage and bone through bone morphogenic protein (BMP), so the BMP is responsible for osteoinductivity
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
General Dentist, MSc Candidate in Periodontology

Study Record Dates

First Submitted

September 23, 2026

First Posted

September 29, 2026

Study Start

April 25, 2025

Primary Completion

August 1, 2026

Study Completion

August 1, 2026

Last Updated

September 29, 2026

Record last verified: 2024-11

Data Sharing

IPD Sharing
Will not share

Locations