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Outcome of Targeted Therapy for Obstructive Sleep Apnea in Children with Obesity and Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD)

Outcome of Targeted Therapy for Obstructive Sleep Apnea in Children with Obesity and Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD)

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
TCTR
Registry ID
TCTR20260726008
Enrollment
140
Registered
2026-07-26
Start date
2026-06-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Targeted treatment of pediatric OSA was associated with significant improvement in sleep-disordered breathing and biochemical markers of liver injury in children with obesity and MASLD. Clinically meaningful improvement in ALT was independently associated with CPAP therapy and better nocturnal oxygenation, supporting the hypothesis that correction of intermittent hypoxemia may contribute to hepatic recovery. These findings identify OSA as a potentially modifiable contributor to pediatric MASLD a

Interventions

Adenotonsillectomy was performed in children with adenotonsillar hypertrophy and moderate-to-severe OSA. Continuous positive airway pressure (CPAP) therapy was prescribed for children with severe OSA
Experimental Procedure/Surgery,No Intervention No treatment
Targeted treatment group,Non-targeted treatment group

Sponsors

Chonburi Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
4 Years to 18 Years

Inclusion criteria

Inclusion criteria: 1. Children aged between 4 and 18 years 2. Obesity is defined as a body mass index (BMI) z-score greater than 2 3. Diagnosis of OSA confirmed by overnight polysomnography 4. Evidence of hepatic steatosis on abdominal ultrasonography

Exclusion criteria

Exclusion criteria: 1. Other liver diseases such as viral hepatitis (hepatitis B or C infection), autoimmune liver disease, or inherited metabolic liver disorders 2. History of use of hepatotoxic medications 3. Chronic systemic diseases known to affect liver function

Design outcomes

Primary

MeasureTime frame
Improvement in liver injury 6 to 12 months after end of the intervention Reduction in serum alanine aminotransferase (ALT) concentration

Secondary

MeasureTime frame
Change in severity of OSA and hepatic steatosis 6 to 12 months after end of the intervention Polysomnographic parameters and hepatic steatosis grade on abdominal ultrasonography

Countries

Thailand

Contacts

Public ContactWoranart Ratanakorn

Chonburi Hospital

woranartr@gmail.com66818192379

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026