Open Sinus Lift Technique With Simultaneous Implantation Using Platelet Rich Fibrin (PRF) Versus Nano-crystalline Hydroxyapatite

Cairo University (CU)

Status: Unknown

Conditions: Atrophied Posterior Maxillary Ridge

Treatments: Procedure: Evaluation of bone quantity in open sinus lift technique with simultaneous implantation ( Nano crystalline hydroxyapatite); Procedure: Evaluation of bone quantity in open sinus lift technique with simultaneous implantation (PRF)

Study type: Interventional

Funder types: Other

Identifiers

NCT02577289

open_sinus_augmentation

Details and patient eligibility

About

Evaluation of bone quantity in open sinus lift technique with space maintaining using platelet rich fibrin (PRF) as sole augmentation material versus nano crystalline hydroxyapatite with simultaneous placing of implants.

Full description

Evaluation of bone quantity in open sinus lift technique with simultaneous implantation using platelet rich fibrin (PRF) versus Nano-crystalline Hydroxyapatite as sole grafting material in patients with atrophied posterior maxillary ridge which provides a new modality for treatment of patients with atrophied posterior maxillary ridge with least cost and a much easier way using platelet rich fibrin (PRF) as substitution to bone graft

Enrollment: 18 estimated patients

Sex: All

Ages: 30 to 70 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• All patients should be seeking for implant supported prosthesis in posterior maxilla bilaterally
• All patients should have atrophied posterior maxillary ridge with the maximum height of the alveolar bone is from 3 mm to 5 mm

Exclusion criteria

• Ongoing steroid therapy;
• Uncontrolled diabetes;
• Recent cardiovascular diseases;
• Inflammation of the maxillary sinus;
• Previous radiant therapy for neoplastic pathologies
• Patient who have had previous failed sinus augmentation, or exhibited pathological finding or had a history of maxillary sinus disease or operations or whose medical condition might increase surgical risk of the research protocol were excluded.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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18 participants in 2 patient groups

Control group ( Hydroxyappetite)

Active Comparator group

Description:

Patients will undergo open sinus lift using nano crystalline hydroxyapatite as augmentation material and placing implants simultaneously then evaluation of bone quantity in open sinus lift technique with simultaneous implantation ( Nano crystalline hydroxyapatite)

Treatment:

Procedure: Evaluation of bone quantity in open sinus lift technique with simultaneous implantation ( Nano crystalline hydroxyapatite)

Test group (PRF)

Experimental group

Description:

Patients will undergo open sinus lift using PRF as sole augmentation material and placing implants simultaneously then Evaluation of bone quantity in open sinus lift technique with simultaneous implantation (PRF)

Treatment:

Procedure: Evaluation of bone quantity in open sinus lift technique with simultaneous implantation (PRF)