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Tumour Regulatory Molecules in Early Pancreatic Cancer Detection

Sponsor: Hull University Teaching Hospitals NHS Trust

NCT ID: NCT03536793

View on ClinicalTrials.gov ↗

At a glance

What the study gets you
Health checks and monitoring — no treatment given
Type of study
Observational (no treatment given)
Time in hospital
In-person visits at study sites — visit count not specified by the sponsor
Drug or intervention
Not specified by the sponsor
How long the study runs
Study runs about 124 months (dates as stated)
About the drug or intervention
Not specified by the sponsor
Patient visit burden
Not specified by the sponsor
Type of study
Observing health over time
Ages
18 Years and over
Who
All
Number of participants
180
Started
2018-10-24
Last checked
2026-06

Plain English Summary

What is this study?

  • • Testing a new treatment for cancer of pancreas
  • • Clinical study - 180 participants
  • • The effective diagnosis of pancreatic cancer is often quite challenging, due to a lack of disease-specific symptoms, resulting in the majority of patients presenting with advanced disease, with an associated dismal prognosis

Who can take part?

  • • Ages 18 Years and over
  • • Diagnosed with cancer of pancreas

Where?

  • • Cottingham - Castle Hill Hospital, Hull University Teaching Hospitals NHS Trust

This is a simplified summary. Always discuss with your doctor before making any decisions.

About This Trial

The effective diagnosis of pancreatic cancer is often quite challenging, due to a lack of disease-specific symptoms, resulting in the majority of patients presenting with advanced disease, with an associated dismal prognosis. Earlier detection of pancreatic cancer, at a stage where surgery is feasible, would greatly increase the 5-year survival rate. Detecting pancreatic cancer early is therefore vital to improve the prognosis for these patients. Pre-cancerous pancreatic cysts are an early indicator of malignant transformation. The ideal screening test would be capable of detecting pancreatic cancer at these initial stages. Current procedures for pancreatic cancer diagnosis are invasive, uncomfortable and costly, and can be considered unnecessary in those cysts found to be benign. We propose to study a number of tumour regulatory molecules that have been the subject of research in laboratories at the University of Hull (e.g., tissue factor (TF), adrenomedullin (AM) using enzyme-linked immunosorbent assays (ELISA) tests) that have been studied in the context of carcinogenic transformation in more common malignancies but have yet to be fully tested in pancreatic malignant transformation. The recent introduction of platform technologies at the University of Hull has broadened this area of investigation by giving us access to next generation genomic sequencing and proteomic analyses of small amounts of tissue samples. We intend to analyse pancreatic cystic fluid samples using these technologies to discover new regulatory molecules. Altogether, his study will measure the levels of novel regulatory molecules and genetic changes involved with pancreatic cancer carcinogenesis using a combination of conventional techniques (e.g. ELISA) and state-of-the-art platform technologies in pancreatic cysts from those patients in whom cancer may be suspected, to determine the potential of these molecules to serve as markers to detect early changes towards pancreatic cancer.

Cancer of PancreasPancreas Cyst

How this trial compares with your answers

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What we know so far

Condition· Matched your search
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Still need:

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Preliminary match based on your answers. Full eligibility requires on-site assessment including medical history, physical exam, and lab tests. This does not guarantee enrolment.

Eligibility at a Glance

Key info

  • Age: 18 Years and over
  • Who can join: All genders

What the study is looking for

  • ✓General
  • ✓Capable of giving written agreement to take part
  • ✓Age ≥18 years
  • ✓Pancreatic Cancer Cohort
  • ✓\- Diagnosed with localised pancreatic cancer amenable to resection (distal pancreatectomy, total pancreatectomy or...

Who cannot take part

  • ✗General
  • ✗Inability to provide written agreement to take part
  • ✗Other known malignant condition, either active or in complete remission ≤5 years
  • ✗HIV, hepatitis C, or any other known communicable disease
See the full criteria
Inclusion Criteria: General * Capable of giving written informed consent * Age ≥18 years Pancreatic Cancer Cohort \- Diagnosed with localised pancreatic cancer amenable to resection (distal pancreatectomy, total pancreatectomy or Whipple's procedure). OR - Diagnosed with inoperable localised pancreatic cancer and referred for further management (malignant control subgroup). Pancreatic Cysts Cohort \- Presence of cystic lesions where MDT have agreed further diagnostic intervention procedures (including FNA/EUS) necessary. OR - Patient the MDT have agreed have resectable lesions suspicious for pancreatic malignancy and going to surgery. Benign Cohort \- Referral for endoscopic cystogastrostomy for complicated acute pancreatitis characterised by peripancreatic fluid collections and pseudocysts in development or matured (non-resolving and requiring further intervention). OR * Referral for cholecystectomy for cholocystitis/chololethiasis. OR * Patient planned to have endoscopy investigation for dyspepsia (normal control subgroup). Exclusion Criteria: General * Inability to provide written informed consent * Other known malignant condition, either active or in complete remission ≤5 years * HIV, hepatitis C, or any other known communicable disease

Where Is This Study? (1 UK site)

Castle Hill Hospital, Hull University Teaching Hospitals NHS Trust

Cottingham HU16 5JQ, United Kingdom

Recruiting
Site contact (verified)

How to Get in Touch

Anthony Maraveyas

Sponsor contact

CONTACT

01482 461245 anthony.maraveyas@nhs.net

James Illingworth

Sponsor contact

CONTACT

01482 461903 james.illingworth3@nhs.net
Data sourced from ClinicalTrials.gov · Last verified: 2026-06