Skip to content

Efficacy and Safety Evaluation of Octreotide in the Treatment of Congenital Hyperinsulinemia

Beijing Children's Hospital, Capital Medical University, National Center for Children's Health

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05171751
Acronym
BCH
Enrollment
50
Registered
2021-12-29
Start date
2021-11-01
Completion date
2021-12-18
Last updated
2021-12-29

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

Conditions

Congenital Hyperinsulinaemic Hypoglycaemia, Octreotide Adverse Reaction

Brief summary

To analyze and evaluate the efficacy and safety of octreotide subcutaneous injection in the treatment of diazazine-ineffective congenital hyperinsulinemia (CHI) in children.

Detailed description

Octreotide subcutaneous injection is effective and safe in the treatment of congenital hyperinsulinemia in children with inefficacy of diazazine.

Interventions

Octreotide subcutaneous injection for congenital hyperinsulinemia with ineffective diazine

Sponsors

Beijing Children's Hospital
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
1 Months to 18 Years
Healthy volunteers
No

Inclusion criteria

1. Consistent with the diagnosis of congenital hyperinsulinemia with ineffective diazine; With the maximum dose of diazine at 15mg/kg/d for 5 days, fasting blood glucose/postprandial blood glucose could not be stabilized at the target value of 3.3mmol/L without intravenous glucose infusion. 2. patients treated with octreotide subcutaneous injection.

Exclusion criteria

1. Before the diagnosis of CHI and the treatment related to CHI, the child had received total pancreatectomy without octreotide 2. Secondary hypoglycemia caused by diseases other than CHI 3. Patients who refused to take octreotide due to parents or family economic reasons, but not hospital treatment factors. 4. Patients who intervene/interfere with octreotide treatment regimen for parental reasons

Design outcomes

Primary

MeasureTime frameDescription
blood glucose1 yearMaintain target blood glucose ≥3.3mmo/L

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026