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Effect of Perioperative Cognitive-Behavioral Intervention on Anxiety, Pain, and Sleep Quality in Children Undergoing Surgical Removal of Impacted Supernumerary Teeth: A Randomized Controlled Trial

Effect of Perioperative Cognitive-Behavioral Intervention on Anxiety, Pain, and Sleep Quality in Children Undergoing Surgical Removal of Impacted Supernumerary Teeth: A Randomized Controlled Trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500110427
Enrollment
Unknown
Registered
2025-10-14
Start date
2025-10-16
Completion date
Unknown
Last updated
2025-10-20

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

Conditions

Supernumerary Tooth

Interventions

Intervention Group:On the basis of conventional treatment and nursing care (including health guidance, preoperative examination, surgical plan explanation, complication education, and perioperative pr
Conventional group:Routine treatment and care (including health guidance, preoperative examinations, explanation of surgical plans, education on complications, and perioperative precautions)

Sponsors

Shenzhen Children's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. General Participant Information: Aged between 6 and 14 years. 2. Diagnosis: Diagnosed with supernumerary teeth via radiographic examination (e.g., panoramic or periapical radiographs) according to the standards outlined in Oral and Maxillofacial Surgery. 3. Treatment Indication: Deemed to have a clear indication for surgical extraction. 4. Organ Function: Normal hepatic and renal function. 5. Cooperation Ability: Normal language, cognitive, and expressive abilities, as well as adequate mouth opening. 6. Informed Consent: Parental/guardian informed consent obtained, with an understanding of the study's process, purpose, and significance.

Exclusion criteria

Exclusion criteria: 1. Patients with any contraindications to surgical treatment. 2. Patients with comorbid congenital diseases. 3. Patients with missing or incomplete clinical data. 4. Patients with other concurrent oral diseases. 5. Patients with coagulation disorders or immune system abnormalities. 6. Patients with severe deficiencies in cognitive, expressive, or comprehensive abilities, or those with strong resistance that would seriously affect the treatment. 7. Patients currently undergoing other treatments that may interfere with the observation of the effect indicators. 8. Patients who have participated in other clinical trials within the past 30 days.

Design outcomes

Primary

MeasureTime frame
Tertiary;

Secondary

MeasureTime frame
postoperative pain;sleep quality;

Countries

China

Contacts

Public ContactZhang Li

Shenzhen Children's Hospital

908357040@qq.com+86 135 3553 9459

Outcome results

None listed

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