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Impact of a Alveolar Ridge Preservation Technique on the Need of Performing Guided Bone Regeneration for Dental Implant Placement

S

Simone Lumetti

Status

Unknown

Conditions

Tooth Avulsion

Treatments

Procedure: Tooth extraction and Alveolar ridge preservation
Procedure: Tooth extraction

Study type

Interventional

Funder types

Other
Industry

Identifiers

NCT04299750
sockpres-13

Details and patient eligibility

About

The aim of this study is to investigate how a socket preservation procedure may reduce the need of guided bone regeneration surgery after tooth extraction and facilitate the placement of a dental implant in the optimal, prosthetic-driven position.

Full description

The main gol of the study is to assess the efficacy of a socket preservation procedure in reducing the need of additional surgeries in order to augment alveolar bone volume before placing a dental implant in optimal position. Bone volume at 6 months will be compared to initial volume in order to assess volume variations and how they affect the positioning of a prosthetically driven, implant.

Enrollment

32 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • at least 18 years of age

    • at least one intercalate tooth to be extracted, with complete alveolus and no soft tissue recession;
    • adequate oral hygiene, i.e. plaque index score ≤10%;
    • mesial-distal width of inter-dental space ≥7 mm;

Exclusion criteria

  • American Society of Anesthesiologists (ASA) score ≥III
  • presence of active periodontitis, clinically diagnosed in presence of probing depths ≥4 mm and bleeding on probing
  • a history of radiotherapy to the head and neck region
  • presence of conditions requiring chronic use of antibiotics
  • medical conditions requiring prolonged use of steroids
  • history of leucocyte dysfunction
  • history of bleeding disorders
  • history of renal failure
  • patients with metabolic bone disorders
  • patients with uncontrolled endocrine disorders
  • disability affecting oral hygiene
  • alcohol or drug abuse
  • HIV infection
  • smoking >10 cigarettes a day or cigar equivalents
  • conditions or circumstances that would prevent completion of study participation
  • mucosal diseases
  • presence of osseous lesions
  • severe bruxing or clenching habits
  • persistent intraoral infections
  • compromised alveolus (dehiscence, etc)

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

32 participants in 2 patient groups

Alveolar Ridge Preservation
Experimental group
Description:
Patients in this arm will undergo atraumatic extraction of an hopeless tooth and a socket preservation procedure. Alveolar ridge preservation will be performed using a slow-resorption bone substitute and a collagen membrane that covers the graft.
Treatment:
Procedure: Tooth extraction and Alveolar ridge preservation
Natural healing
Active Comparator group
Description:
Patients in this arm will undergo atraumatic extraction of an hopeless tooth. The socket will follow natural healing.
Treatment:
Procedure: Tooth extraction

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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