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Photoacoustic-steaming Unite Miminal-invasive Chemomechanical-preparation Hydramatic-obturation (PUMCH) root canal therapy in pulptitis: a non-inferiority, randomized controlled clinical trial

Clinical validation of Photoacoustic-steaming Unite Miminal-invasive Chemomechanical-preparation Hydramatic-obturation root canal therapy - Clinical validation of PUMCH root canal therapy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200064355
Enrollment
Unknown
Registered
2022-10-04
Start date
2022-09-30
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

pulptitis

Interventions

conventional root canal therapy:conventional root canal therapy
PUMCH therapy:PUMCH root canal therapy

Sponsors

Peking Union Medical College Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Outpatient diagnosis of pulpitis; 2. premolar or molar with four walls of the affected tooth is intact or single-wall defect; 3. Aged between 18-60 years, no gender limitation; 4. Good oral hygiene; 5. Can sign an informed consent form.

Exclusion criteria

Exclusion criteria: 1. Serious systemic diseases (such as uncontrolled diabetes, cardiovascular diseases, immune disorders, blood diseases, etc.); 2. Pregnant or lactating patients; 3. Patients with mental illness or a history of mental illness; 4. Patients with infectious diseases (such as hepatitis, syphilis, AIDS patients, etc.); 5. Patients with head and neck tumors, or after radiotherapy of tumor head and neck; 6. Patients who have taken antibiotics in the past three months; 7. Patients with moderate to severe periodontitis; 8. Patients with abnormal salivary gland function; 9. Patients with temporomandibular joint disorder; 10. Patients with night grinding or severely abnormal occlusion; 11. Patients with acid erosion and severe caries.

Design outcomes

Primary

MeasureTime frame
X-ray of periapical region;

Secondary

MeasureTime frame
Patient visual self-rating;Patient oral scores;

Countries

China

Contacts

Public ContactXinyu He

Peking Union Medical College Hospital

hexinyupumch@126.com+86 13811818250

Outcome results

None listed

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