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PIRAMID study

Development of diagnostics for pancreatic cancer's molecular resection margin status at dissected peripancreatic tissue margin by margin imprint droplet digital PCR - PIRAMID study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-jRCT1041230160
Enrollment
200
Registered
2024-02-28
Start date
2022-01-31
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Pancreatic Cancer

Interventions

None listed

Sponsors

Kodera Yasuhiro
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Patients with pancreatic cancer diagnosed and resected by various imaging and pathological diagnoses between January 1, 2017 and December 31, 2025. (2) Patients whose prognosis for life is judged to be more than 6 months by the study investigator (3) Patients whose age at the time of enrollment is between 20 and 90 years old (3) Patients must be between 20 and 90 years of age at the time of enrollment. (4) Performance status (ECOG) is 0, 1, or 2. (5) Patients must have undergone first resection for pancreatic cancer. (6) Consent for participation in this study has been obtained from the patient (For the use of stored specimens (Study No. 2014-0042) collected at Nagoya University Hospital for a different purpose from the study and for which consent for secondary use has already been obtained, please contact the Department of Gastroenterological Surgery, Nagoya University Graduate School of Medicine, and the Department of Gastroenterology, Oncology and General Surgery, Department of Medicine, Faculty of Academic Research, University of Toyama, Nagoya Medical Center, and the opportunity to refuse will be guaranteed by disclosing the information on the website of the Clinical Research Center).

Exclusion criteria

Exclusion criteria: (1) Patients whose prognosis for life is judged to be less than 6 months by the study investigator (ii) Patients with serious (still requiring hospitalization) underlying diseases (cardiac disease, pulmonary disease, intestinal paralysis, intestinal obstruction, diabetes mellitus difficult to control, renal failure, cirrhosis of the liver, etc.) (iii) Active multiple cancers (simultaneous multiple cancers and iatrogenic multiple cancers with a disease-free period of less than 5 years. (c) Active overlapping cancer (simultaneous overlapping cancer and iatrogenic overlapping cancer with a disease-free period of less than 5 years; however, carcinoma in situ (intraepithelial carcinoma) and intramucosal carcinoma equivalent lesions judged to have been cured by local treatment are not included in active overlapping cancer). (iv) Patients with psychosis or psychiatric symptoms that would make participation in the study difficult. (v) Patients who did not give consent to participate in the study (vi) Other patients who are judged to be inappropriate for this study by the investigator (subinvestigator).

Design outcomes

Primary

MeasureTime frame
Relationship between mR status and risk of local recurrence and life expectancy

Secondary

MeasureTime frame
Relationship between mR status and pathological findings, and comparison of local recurrence and prognostic value between mR status and allele frequency of KRAS mutations in cfDNA

Contacts

Public ContactHaruyoshi Tanaka

Nagoya University

tanakaharu@med.nagoya-u.ac.jp+81-52-744-2245

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026