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A Randomized Controlled Clinical Study to Evaluate the Safety and Efficacy of Hyaluronic Acid Gel Loaded with Dental Follicle Stem Cell Exosomes in the Treatment of Periodontitis

A Randomized Controlled Clinical Study to Evaluate the Safety and Efficacy of Hyaluronic Acid Gel Loaded with Dental Follicle Stem Cell Exosomes in the Treatment of Periodontitis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600123797
Enrollment
Unknown
Registered
2026-04-29
Start date
2026-04-29
Completion date
Unknown
Last updated
2026-05-04

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

Conditions

Periodontitis

Interventions

Control group:Hyaluronic acid gel without loading the exocrine body of dental follicle stem cells
Experimental group:Hyaluronic acid gel loaded with exocrine body of dental follicle stem cells

Sponsors

The First People's Hospital of Yunnan Province
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. The age range is from 18 to 60 years old, inclusive of the boundaries, regardless of gender. 2. The subjects meet the diagnostic criteria for periodontitis stage III/IV (International New Classification of Periodontal and Peri-implantitis Diseases in 2018). 3. The clinical probing depth of the tested teeth is >= 5mm and the radiographic examination reveals a subgingival pocket of >= 2mm, with a mobility of = 2mm. 4. The subjects have given informed consent, understand the purpose of this trial, and can cooperate with the trial requirements and undergo regular follow-up for at least 6 months after the treatment. 5. The subjects can achieve good self-plaque control, including correct brushing and proper use of dental floss, etc.

Exclusion criteria

Exclusion criteria: 1. Those with severe periodontal disease (alveolar bone resorption exceeding two-thirds of the tooth root length) or whose occlusal trauma affects the interpretation of the research results; 2. Those with a distance from the lowest point of the periodontal pocket beneath the tooth to the root apex 7.0% within 3 months before screening; 7. Smokers (smoking >= 10 cigarettes per day within 6 months before screening); 8. Those with uncontrollable systemic infections; 9. Those who, in the researcher's judgment, are not suitable to participate or have withdrawn the informed consent form.

Design outcomes

Primary

MeasureTime frame
The improvement value of the periodontal clinical attachment level at the 6th month after the surgery;

Secondary

MeasureTime frame
The positive rate of bleeding detected by probing at the 6th month after the operation;Improvement value of gum recession at the 6th month after surgery;The improvement of root bifurcation lesion grading at the 6th month after the surgery;The improvement in tooth looseness at the 6th month after the surgery;The depth of bone defect repair at the 6th month after the surgery;The increase in the area of keratinized gingiva at the 6th month after the surgery;The increase in the filling of the gingival papillae at the 6th month after the operation;Patient's subjective perception evaluation;

Countries

China

Contacts

Public ContactJianhong Hou

The First People's Hospital of Yunnan Province

18808713303@163.com+86 871 63638020

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 7, 2026