Prediction of Clinical Outcomes in Patients with Intestinal Perforation by Abdominal Bacteriomics and Fungomics

Status

Recruiting

Phases

Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2400085235

Enrollment

Unknown

Registered

2024-06-03

Start date

2023-04-09

Completion date

Unknown

Last updated

2024-07-08

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

Conditions

Severe intestinal perforation patients

Interventions

Case series:none

Eligibility

Sex/Gender

All

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Continuous collection of adult patients (aged 18 and above) admitted to Zunyi Medical University from July 2023 to July 2025 with intestinal perforation; The patient underwent emergency surgery and was diagnosed with intestinal perforation; The patient's family members have informed consent and signed to participate in this clinical study.

Exclusion criteria

Exclusion criteria: Patients or family members refuse to participate in this study; Patients who are expected to die within 48 hours or stay in the ICU for less than 48 hours; Patients undergoing organ transplantation; Pregnant patients; Patients who donate organs.

Design outcomes

Primary

Measure	Time frame
28 day mortality rate;	—

Countries

China

Contacts

Public ContactXing Zhouxiong

Zunyi Medical University Affiliated Hospital

xingzhouxiong111@126.com+86 155 9776 0160

Outcome results

None listed

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