NCT06275789

Brief Summary

The purpose of the study is to compare a new grafting material for alveolar ridge preservation to a commonly used and well studied material. Alveolar ridge dimensions as well as histology will be compared.

Trial Health

77
On Track

Trial Health Score

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

Enrollment
30

participants targeted

Target at below P25 for not_applicable

Timeline
1mo left

Started Jan 2024

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

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 Progress97%
Jan 2024Jun 2026

Study Start

First participant enrolled

January 26, 2024

Completed
12 days until next milestone

First Submitted

Initial submission to the registry

February 7, 2024

Completed
16 days until next milestone

First Posted

Study publicly available on registry

February 23, 2024

Completed
2.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2026

Last Updated

September 12, 2025

Status Verified

September 1, 2025

Enrollment Period

2.3 years

First QC Date

February 7, 2024

Last Update Submit

September 5, 2025

Conditions

Outcome Measures

Primary Outcomes (2)

  • changes in horizontal dimensions of the alveolar ridge

    Soft and hard tissue horizontal dimensions of the alveolar ridge will be measured after extraction and 4 months later.

    4 months

  • changes in vertical dimensions of the alveolar ridge

    Soft and hard tissue vertical dimensions of the alveolar ridge will be measured after extraction and 4 months later.

    4 months

Secondary Outcomes (1)

  • vital bone percentage

    4 months

Other Outcomes (6)

  • thickness of the buccal plate in mm and its influence on the ridge dimension

    4 months

  • the thickness of the lingual plate in mm and its influence on the ridge dimension

    4 months

  • the thickness of the overlying buccal soft tissue in mm and its influence on the ridge dimension

    4 months, 1 year

  • +3 more other outcomes

Study Arms (2)

Test Group

EXPERIMENTAL

This group will receive the grafting material that is a combination of DFDBA + DBBM + collagen matrix seal during the alveolar ridge preservation procedure.

Procedure: Alveolar ridge preservation

Control Group

ACTIVE COMPARATOR

This group will receive the grafting material that is a Tutoplast® processed mineralized particulate allograft + collagen matrix seal during the alveolar ridge preservation procedure.

Procedure: Alveolar ridge preservation

Interventions

Premolar tooth will be extracted flapless and ridge preservation procedure with bone grafting material will be done.

Control GroupTest Group

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Patients in good health
  • Require the extraction of at least one premolar or molar with future implant placement
  • Sufficient keratinized gingiva (equal or more than 2mm prior to extraction),
  • No more than 3mm of buccal bone loss
  • Flapless extraction possible
  • Full mouth plaque index of less than 25%

You may not qualify if:

  • Nicotine consumption equivalent to or more than 10 cigarettes per day
  • Electronic cigarette usage
  • A history of irradiation of head and neck area
  • Immunodeficiency disease
  • Uncontrolled systemic health problems (hypertension crisis 180/120, hyperthyroidism, diabetes with HbA1c over 7, recent history of stroke, cancer) History of medications that affect bone remodeling process (bisphosphonates, RANK-L inhibitors)
  • Previous adverse reaction to the biomaterials used
  • Pregnancy/lactation, or those who are trying to become pregnant.
  • Active uncontrolled or untreated periodontal disease
  • Periapical lesions greater than 1 cm and soft tissue pathology

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Nova Southeastern University

Fort Lauderdale, Florida, 33328, United States

RECRUITING

Related Publications (45)

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    PMID: 15882225BACKGROUND
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    PMID: 30623987BACKGROUND
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    PMID: 25415247BACKGROUND
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Central Study Contacts

Andee Goldstein, DMD

CONTACT

Fatemeh Samavatijame, DMD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

February 7, 2024

First Posted

February 23, 2024

Study Start

January 26, 2024

Primary Completion (Estimated)

June 1, 2026

Study Completion (Estimated)

June 1, 2026

Last Updated

September 12, 2025

Record last verified: 2025-09

Data Sharing

IPD Sharing
Will not share

Locations