Freeze-deried (FD) PRP for bone engineering

JRCT ID: jRCTs072180076

Registered date:26/03/2019

Basic Information

• Recruitment status: Complete
• Health condition(s) or Problem(s) studied: alveolar bone atrophy
• Date of first enrollment: 20/02/2018
• Target sample size: 5
• Study type: Interventional

Intervention(s)

Intervention period: 4weeks
Intervention volume: maximum 90ml of peripheral blood for providing FD-PRP
Number of times of Intervention: 1 time

Outcome(s)

• Primary Outcome: Safety (including the adverse events)
• Secondary Outcome: None

Key inclusion & exclusion criteria

• Age minimum: >= 20age old
• Age maximum: <= 75age old
• Gender: Both

Include criteria

1. Patients who are partially or fully edentulous, and are required to treat by dental implants for prosthetic rehabilitation.
2. Patients who have insufficient bone height and/or width to place the dental implant
3. Patients who received the oral health care and maintain the good condition of Plaque Control.
4. The age of the patients: 20- to 75-years old

Exclude criteria

1. All patients are required to be nonsmokers.
2. Patients who have systemic disease, malignances, chronic infections, immune system abnormalities, septicemia, syphilis, HBV, HCV, HTLV-1, HIV, pregnancy, dementia.
3. Patients who have disorder of blood coagulation.
4. Patients who have hepatitis function disorders, metabolic bone disease or skeletal dysplasia.
5. Patients who needs the legal representative.

Related Information

• Primary Sponsor: Asahina Izumi
• Secondary ID(s): UMIN000027144