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Evidence-Based Evaluation of the Efficacy and Safety of Drugs for the Treatment of Clonorchiasis in Guangxi Region

Evidence-Based Evaluation of the Efficacy and Safety of Drugs for the Treatment of Clonorchiasis in Guangxi Region

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600126085
Enrollment
Unknown
Registered
2026-06-03
Start date
2025-12-30
Completion date
Unknown
Last updated
2026-06-08

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

Conditions

Clonorchiasis (Clonorchis sinensis infection)

Interventions

Albendazole group:None
Praziquantel group:None

Sponsors

The People’s Hospital of Guangxi Zhuang Autonomous Region
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients diagnosed with clonorchiasis by detecting Clonorchis sinensis eggs or worms in fecal examinations or biliary drainage fluid; 2. Patients who received standard treatment with albendazole and praziquantel at the research center from January 2023 to March 2025; 3. Patients with complete medical records, including diagnostic evidence, medication regimens, post-treatment egg test results, and safety records.

Exclusion criteria

Exclusion criteria: 1. Patients with incomplete data records, for whom the efficacy/safety indicators cannot be clearly identified; 2. Patients co-infected with other parasites; 3. Patients who changed medications, discontinued treatment, or failed to complete follow-up during the treatment period.

Design outcomes

Primary

MeasureTime frame
Egg negative conversion rate;

Countries

China

Contacts

Public ContactZhang Li

The People’s Hospital of Guangxi Zhuang Autonomous Region

30173359@qq.com+86 771 2186165

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 11, 2026