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Clinical study of autologous dental pulp stem cell complex combined with exosomes transplantation for periodontal tissue regeneration

Clinical study of autologous dental pulp stem cell complex combined with exosomes transplantation for periodontal tissue regeneration

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900027140
Enrollment
Unknown
Registered
2019-11-01
Start date
2019-11-01
Completion date
Unknown
Last updated
2019-12-16

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

Conditions

Chronic Periodontitis

Interventions

Experimental Group1:Dental pulp stem cell complex + Bio-Oss bone meal
Experimental Group2:Dental pulp stem cell + exosome complex + Bio-Oss bone meal
Control group:Bio-Oss bone meal

Sponsors

College of Stomatology,Xi'an Jiaotong University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: 1) Age 18 to 55 years old; 2) at least one tooth in the mouth has a 2 or 3 wall vertical type intrabony defects with PD>=5mm and the imaging bone defect depth is >=3mm; 3) The tooth looseness studied is within II (including II degree), and there is enough attachment width to meet GTR and bone grafting; 4) There are teeth in the patient's mouth that can remove healthy pulp tissue (such as impacted wisdom teeth or non-functional teeth); 5) After guidance, have a good sense of oral care; 6) Those who understand the purpose of this study and agree to sign the informed consent form. [Note] Imaging depth of the inner wall defect refers to the linear distance between the highest point and the lowest point of the bone defect on the X-ray film.

Exclusion criteria

Exclusion criteria: 1) Smokers (more than 10 in the past 3 months); 2) Patients with systemic diseases who cannot undergo surgery are not included. For example, patients with acute heart attack within six months, patients with rheumatic heart disease, patients with blood diseases, patients with uncontrolled diabetes (fasting blood glucose >8.88mmol/L), patients with infectious diseases, history of malignant tumors, and people with mental disorders And severely malnourished (serum albumin concentration <2 g/dL)); 3) Allergies and history of allergies to blood products; 4) breastfeeding, pregnant women; 5) taking calcium antagonists 4 weeks before surgery; 6) Those who need to take adrenal corticosteroids within 4 weeks after surgery; 7) are participating in other clinical trials; 8) Others of this project believe that the test does not meet the requirements of this test.

Design outcomes

Primary

MeasureTime frame
bone defect depth (BDD);

Secondary

MeasureTime frame
probing depth (PD);clinical attachment loss (CAL);gingival recession (GR);

Countries

China

Contacts

Public ContactLi Ang

College of Stomatology, Xi'an Jiaotong University

drliang@mail.xjtu.edu.cn+86 15702988704

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026