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Study on the Mogroside in Ameliorating Olanzapine-induced Hyperglycemia

Study on the Mogroside in Ameliorating Olanzapine-induced Hyperglycemia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026001397
Enrollment
Unknown
Registered
2026-06-03
Start date
2026-06-01
Completion date
Unknown
Last updated
2026-06-22

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

Conditions

Olanzapine-induced hyperglycemia

Interventions

Intervention Group:Mogroside 100 mL per sachet, 3 times daily, 1 sachet each time, for 8 weeks
follow-up for another 8 weeks
Waiting-list Group:Follow-up for 8 weeks
then Mogroside 100 mL per sachet, 3 times daily, 1 sachet each time, for 8 weeks

Sponsors

Shanghai Mental Health Center
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) Meets the diagnostic criteria for schizophrenia according to the International Classification of Diseases, 10th Revision (ICD-10); (2) Fixed dose of olanzapine for at least 1 month; (3) Fasting blood glucose =6.1 mmol/L and not on any antidiabetic medications; (4) Age between 45-65 years, both genders; (5) Provides written informed consent to participate in this study.

Exclusion criteria

Exclusion criteria: (1) Pregnant or lactating women; (2) Severe somatic diseases; (3) Currently using drugs such as clozapine, SSRIs, or SNRIs that increase the risk of hyperglycemia; (4) Other conditions affecting blood sugar or currently using antidiabetic medications.

Design outcomes

Primary

MeasureTime frame
Fasting Blood Glucose;

Secondary

MeasureTime frame
Height;Body-weight;blood lipids;HBA1c;Liver functions;16S rDNA sequencing;Gastrointestinal motility;

Countries

China

Contacts

Public ContactChao Luo

Shanghai Mental Health Center

superluo2009@126.com+86-15078819863

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Jun 29, 2026