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Evaluation of spontaneous peritonitis in patients with cirrhosis using next-generation sequencing (NGS)

Evaluation of spontaneous peritonitis in patients with cirrhosis using next-generation sequencing (NGS)

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CRIS
Registry ID
KCT0008935
Enrollment
200
Registered
2023-11-10
Start date
2021-11-11
Completion date
Unknown
Last updated
2023-11-13

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

Conditions

None listed

Interventions

None listed

Sponsors

Soon Chun Hyang University Hospital Bucheon
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. When spontaneous bacterial peritonitis is suspected despite ascites due to underlying liver cirrhosis 1. If there is ascites due to underlying liver cirrhosis and spontaneous bacterial peritonitis is not suspected. 2. Age from 19 years old to 79 years old 3. Patients who sign a written consent form prior to study participation and understand that they have the right to withdraw their consent from study participation at any time without penalty. 4. Patients with archival specimens available for genetic analysis or patients eligible for specimen collection for genetic analysis.

Exclusion criteria

Exclusion criteria: 1. Patients who refuse to participate in clinical trials 2. When collecting multiple urine samples cannot be performed aseptically 3. When it is difficult to collect a stool sample 4.Patients with a history of uncontrolled seizures, central nervous system disorders, or psychiatric disorders judged to be clinically significant by the examiner

Design outcomes

Primary

MeasureTime frame
Differentiation of causative bacteria using next-generation nucleotide sequence analysis

Secondary

MeasureTime frame
Sensitivity comparison with existing testing methods

Countries

Korea, Republic of

Contacts

Public ContactJeong-Ju Yoo

Soon Chun Hyang University Hospital Bucheon

puby17@naver.com+82-32-621-5065

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026