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Longitudinal Evolution of Symptom Clusters and Identification of Core Symptoms in Patients with Severe Acute Pancreatitis

Longitudinal Evolution of Symptom Clusters and Identification of Core Symptoms in Patients with Severe Acute Pancreatitis

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600123880
Enrollment
Unknown
Registered
2026-04-30
Start date
2026-05-05
Completion date
Unknown
Last updated
2026-05-04

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

Conditions

Severe Acute Pancreatitis

Interventions

Observation group:None

Sponsors

Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Aged >= 18 years. 2.Meet the diagnostic criteria for Severe Acute Pancreatitis (SAP) as defined in the Guidelines for Diagnosis and Treatment of Acute Pancreatitis in China (2021): (1) Persistent upper abdominal pain; (2) Serum amylase and/or lipase levels >= 3 times the upper limit of normal; (3) Diagnosis confirmed by abdominal CT or other imaging modalities; (4) Persistent (> 48h) organ failure, defined as a modified Marshall score > 2. A diagnosis of SAP is established if the patient meets at least two of the first three criteria, along with the fourth criterion. 3.Length of stay in the Intensive Care Unit (ICU) > 72 hours. 4.Voluntary participation in this study with a signed informed consent form (ICF). If the subject is unable to read and sign the ICF due to lack of behavioral capacity or other reasons, their legal guardian/authorized representative must act as a proxy for the informed consent process and sign the ICF on their behalf.

Exclusion criteria

Exclusion criteria: 1.Patients with other severe underlying diseases, such as cardiac, hepatic, pulmonary, or renal dysfunction/insufficiency, and malignant tumors. 2.Vulnerable populations (other than critically ill patients), including those with psychiatric disorders, cognitive impairments, pregnant women, and illiterate individuals.

Design outcomes

Primary

MeasureTime frame
Physical symptoms;Social Support;Cognitive and Behavioural Responses;Visceral Sensitivity Index;Self-efficacy;Illness Perception;

Countries

China

Contacts

Public ContactHuang Jingying

Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University

3407109@zju.edu.cn+86 577 6684741

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 7, 2026