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Multimodal Digital Postoperative Education for Reducing Complications in Pediatric Endodontics: A Multicenter Randomized Controlled Trial Protocol

Multimodal Digital Postoperative Education for Reducing Complications in Pediatric Endodontics: A Multicenter Randomized Controlled Trial Protocol

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600128353
Enrollment
Unknown
Registered
2026-07-17
Start date
2026-09-01
Completion date
Unknown
Last updated
2026-07-20

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

Conditions

Pediatric Pulp Diseases

Interventions

Intervention group:Multimodal digital postoperative oral health education
Control group:Traditional verbal education + paper?based leaflets

Sponsors

Xuzhou Stomatological Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
3 Years to 12 Years

Inclusion criteria

Inclusion criteria: 1. Children aged 3–12 years with pulp lesions of primary or young permanent teeth confirmed by clinical and imaging examinations, who meet the treatment indications for pulpotomy or pulpectomy. 2. Children are in good physical condition and can cooperate with dental treatment and postoperative follow-up. 3. Accompanying caregivers have normal communication skills, can proficiently use smartphones and WeChat, and can fully cooperate with the study. 4. Caregivers are fully informed and voluntarily sign the informed consent form; children aged 7 years and above need to sign the child assent form. 5. Children can ensure 12-month standardized postoperative follow-up with no relocation plans.

Exclusion criteria

Exclusion criteria: 1. Children complicated with systemic diseases such as congenital heart disease, immunodeficiency, coagulation disorders, and mental retardation, who are unable to cooperate with treatment or interfere with efficacy evaluation. 2. The affected teeth present root resorption, internal resorption, or extensive periapical destruction with extremely poor prognosis. 3. Caregivers have no smartphone, cannot use WeChat, or have cognitive impairment and are unable to understand health education content. 4. Those who plan to leave the local area within 12 months and cannot complete the full follow-up. 5. Participating in other clinical trials simultaneously, which may affect the data evaluation of this study. 6. Other circumstances deemed inappropriate for enrollment by the researchers.

Design outcomes

Primary

MeasureTime frame
12?month incidence of postoperative complications after pediatric endodontic treatment;

Secondary

MeasureTime frame
Post?operative education satisfaction of children’s caregivers;Mastery of postoperative oral health education knowledge;Post?operative oral hygiene compliance;

Countries

China

Contacts

Public ContactXie Ni'na

Xuzhou Stomatological Hospital

375162590@qq.com+86 516 8396 5900

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jul 23, 2026