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Differential diagnosis of pancreatic cancer and chronic pancreatitis with serum miR-25

A prospective study of serum miR-25 detection in differential diagnosis of pancreatic cancer and chronic pancreatitis

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000037002
Enrollment
Unknown
Registered
2020-08-26
Start date
2020-10-01
Completion date
Unknown
Last updated
2020-09-28

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

Conditions

pancreatic cancer

Interventions

Gold Standard:Pancreatic cancer: pancreatic ductal adenocarcinoma originating from pancreatic ductal epithelium was confirmed by pathological examination (operative biopsy, puncture biopsy, cytologica
Index test:Serum miR-25

Sponsors

The First Affiliated Hospital of the Naval Medical University of the Chinese People's Liberation Army
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Patients diagnosed as pancreatic cancer and chronic pancreatitis in the Department of Hepatobiliary Pancreatic and Splenic Surgery and the Department of Gastroenterology in our hospital from October 2020 to June 2022 were included in the study strictly according to the inclusion criteria. Study group: (1) 18-75 years old, male or female. (2) Pancreatic ductal adenocarcinoma originating from pancreatic ductal epithelium was confirmed by pathological examination (operative biopsy, puncture biopsy, cytological examination). Pancreatic ductal adenocarcinoma was highly suspected to be pancreatic cancer by clinical diagnosis before (pancreatic ductal adenocarcinoma, PDAC), and patients with pancreatic ductal adenocarcinoma diagnosed by surgical biopsy and blood collection before operation could be enrolled in the group. (3) before blood collection, the patient did not receive surgical treatment. (4) before blood collection, the patient had not received systematic antineoplastic drugs (Systematic Anti-tumor Therapy), including long-acting growth inhibitor analogues, interferon, PRRT (peptide receptor radionuclide therapy), mTOR inhibitors and chemotherapy, etc. (5) before blood collection, the patient did not receive radiotherapy or neoadjuvant therapy. (6) sign the informed consent form for research. Control group: (1) 18-75 years old, male or female. (2) patients who are clinically diagnosed as chronic pancreatitis and have no evidence to support the diagnosis of pancreatic cancer. (3) Blood samples were collected before admission. (4) sign the informed consent form for research.

Exclusion criteria

Exclusion criteria: (1) the subjects were in the stage of acute infection. (2) the subjects had been treated or taken drugs before blood collection. (3) failed to join the group or refused to follow up for various reasons.

Design outcomes

Primary

MeasureTime frame
pancreatic cancer;SEN, SPE, ACC, AUC of ROC;

Countries

China

Contacts

Public ContactLiu Wenyu

The First Affiliated Hospital of the Naval Medical University of the Chinese People's Liberation Army

lwywinner@hotmail.com+86 13818654423

Outcome results

None listed

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