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NCT Number: NCT06626776

The Use of Extended Platelet Rich Fibrin in Lateral Sinus Augmentation

thirty implants will be inserted in patients seeking implantation of their lost posterior maxillary teeth (premolar and molars) with limited bone height below the floor of the maxillary sinus, secondary to sinus pneumatization. The patients will be selected from those attending the outpatient clinic of the Oral & Maxillofacial Surgery Department, Faculty of Dentistry, Mansoura University.

1. Clinical Evaluation

• Implant stability 2. Radiographic Evaluation Vertical bone gain (VBG)

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Key information

Conditions

Sinus Lift Augmentation

Age range

20 year–60 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

MANSOURA University

Al Mansurah, Egypt

Location contact

mansoura

CONTACT

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patent ostium of maxillary sinus.
  • Patient with missing one or more posterior maxillary teeth.
  • Residual bone height of 3-6 mm, measured from the crest of alveolar ridge to the floor of the maxillary sinus at the planned implant site.
  • A ridge width at the site of implantation of <5mm.
  • Platelets of normal range.
  • Good oral hygiene.
  • Patients in the age frame between 20 years and 60 years old.
  • No gender preface in selection of the patients.
  • A minimum crown height space of 8 mm.

Exclusion criteria

  • Active sinusitis, cyst, tumors or root tips at the planned surgical site.
  • Patients with systemic diseases that contra-indicate the surgical procedure such as uncontrolled diabetes mellitus, bleeding disorders, serious osseous disorders, and mental disorders.
  • Heavy smoking and alcoholism.
  • Parafunctional habits such as bruxism and clenching.
  • Signs of acute infection or pus discharge.
  • Disturbed occlusion.

Treatment and study plan

lateral sinus lift with using allograft and collagen membrane

Procedure

sinus floor elevation with placing allograft and collagen membrane

lateral sinus lift with using exteneded platelet rich fibrin

Procedure

sinus floor elevation with placing eprf

Primary outcomes

  1. implant stability

    Time frame: 9 months

    the stability of the implants will be evaluated by RFA with the Osstell Mentor device.

  2. Vertical bone height

    Time frame: 6 months

    vertical bone height will be measured as the distance from the alveolar crest to the new sinus floor at the middle of the implant

Study contacts

Contact information is provided by the study sponsor or research team.

ammar samman

CONTACT

[email protected]

+201558990325

Sponsors and collaborators

Lead sponsor

Mansoura University

Other

Registry information

Official study title

Extended Platelet Rich Fibrin in Lateral Maxillary Sinus Lifting With Simultaneous Implant Placement.

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Oct 4, 2024
Registry last updated
Oct 4, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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