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Impact of prolonged propranolol use on cognitive abilities and sleep quality in children with infantile hemangioma

Impact of prolonged propranolol use on cognitive abilities and sleep quality in children with infantile hemangioma

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600118284
Enrollment
Unknown
Registered
2026-02-04
Start date
2026-02-05
Completion date
Unknown
Last updated
2026-02-09

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

Conditions

infantile hemangioma

Interventions

Infantile Hemangioma Group Treated with Oral Propranolol:None
Control groupe:None

Sponsors

West China Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
0.2 Years to 6 Years

Inclusion criteria

Inclusion criteria: Inclusion Criteria for Infants with Hemangiomas Treated with Oral Propranolol: 1. Meet the clinical diagnostic and treatment criteria requiring oral propranolol therapy for infantile hemangiomas; 2.Have not taken any neurological or psychiatric medications affecting sleep within the past 6 months; 3. Legal guardian consents to participate in this study. Inclusion Criteria for the Control Group: 1. Infants who do not require oral propranolol treatment for hemangiomas; 2. No sleep disorders or other neurological or psychiatric diseases; 3. Have not taken any neurological or psychiatric medications affecting sleep within the past 6 months; 4. Legal guardian consents to participate in this study.

Exclusion criteria

Exclusion criteria: Exclusion Criteria for Participants: 1. History of other severe psychiatric disorders, such as schizophrenia; 2. History of other confirmed organic brain diseases, such as epilepsy, traumatic brain injury, encephalitis, etc.; 3. Presence of intracranial metal implants or implanted medical devices (e.g., pacemakers); 4. Diagnosis of confirmed genetic or metabolic disorders, such as Down syndrome, Fragile X syndrome, Angelman syndrome, etc.; 5. Currently taking neurological or psychiatric medications that affect sleep, or having discontinued such medications for less than six months; 6. Inability to cooperate with polysomnography (PSG) monitoring.

Design outcomes

Primary

MeasureTime frame
Sleep Monitoring;Denver Developmental Screening Test II;

Secondary

MeasureTime frame
Infant Sleep Habits Questionnaire;World Health Organization Infant and Toddler Developmental Assessment Tool;Mullen Scales of Early Learning;Assessment of brain function;

Countries

China

Contacts

Public ContactYanan Li

West China Hospital of Sichuan University

yananli@scu.edu.cn+86 28 8542 1805

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 15, 2026