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A clinical study for validity and provision method of periodontal tissue regeneration with autologous adipose derived stem cells and platelet rich plasma

A clinical study for validity and provision method of periodontal tissue regeneration with autologous adipose derived stem cells and platelet rich plasma - Periodontal tissue regeneration using adipose derived stem cells and platelet rich plasma

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000036232
Enrollment
20
Registered
2019-03-17
Start date
2019-03-18
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

periodontitis

Interventions

Transplantation of the processed cells Administration of Enamel matrix derivative

Sponsors

Juntendo University
Lead Sponsor
Juntendo clinical research and trial ceter, Juntendo hospital
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: A patient MUST: 1)Have a Periodontal pocket more than 5 mm at baseline examination. 2) Intrabony defect is 5 mm and more depth, and 2 mm and more width at interproximal site of the experimental tooth by X-ray examination. 3)Already have received initial preparation at the screening. 4)Mobility of experimental tooth is 0, 1, or 2, and exist keratinized gingiva. 5)Good oral health. 6)Subcutaneous fat tissue can be harvest normally and safely 7)20 years and older. 8)Signed informed consent.

Exclusion criteria

Exclusion criteria: Patient MUST NOT: 1)Can not be measured clinical attachment level of experimental tooth. 2)Have a history of Complicate malignant tumor. 3)Suspected of oral malignant tumor or precancerous lesion. 4)Have a history of usage bisphosphonate, or necessary. 5)Need to undergo the treatment, such as surgical treatment, restorative treatment or root canal treatment, at the experimental tooth within 36 weeks after transplant. 6)Pregnancy, during breastfeeding, or possibility of pregnancy. 7)Have disease of kidney, liver and/or blood. 8)Hemoglobin A1c is more than 6.8% at the screening. 9)Have active infectious diseases. 10)Alcoholism or Drug dependence. 11)Mental or consciousness disorder. 12)HCV antibody, HBs antigen, ATLA virus antibody or HIV antibody positive person. 13)Smoke more than 10 pieces per day. 14)Other,the investigator believes makes him/her unsuitable for participation in the clinical study.

Design outcomes

Primary

MeasureTime frame
Validity and efficacy

Secondary

MeasureTime frame
Safety

Countries

Japan

Contacts

Public ContactMorikuni Tobita

Juntendo University Hospital Department of Oral and Maxillofacial Surgery

mtobita@juntendo.ac.jp03-3813-3111

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026