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Serum Uric AcidNCT07091526

Whether Control of Serum Uric Acid (SUA) Improves Survival After Pancreatic Cancer

An observational study of Serum Uric Acid, run by Hepatopancreatobiliary Surgery Institute of Gansu Province at 1 site in China.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

This retrospective study aims to analyze the impact of postoperative changes in serum uric acid (SUA) levels on the prognosis of patients undergoing pancreatic cancer resection. Read more about this study

Who is it for?
Ages 18 to 85 years
Conditions the study is for
Serum Uric Acid
What is being tested?
serum uric acid test
How many people
168 participants
Where
1 siteChina
Study dates
29 Jul 2025to 29 Dec 2026
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 85 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Radical pancreatic cancer resection patients

Who may be able to join

  • Patients with pathologically confirmed pancreatic cancer (primary)
  • Patients who underwent Radical resection of pancreatic cancer(Pancreaticoduodenectomy or Distal pancreatectomy)
  • The postoperative survival time was at least 6 weeks

Who cannot join

  • No surgery was performed, or only palliative surgery/ biopsy was performed
  • Patients who underwent emergency hemodialysis or plasma exchange after surgery
  • History of gout or long-term urate-lowering therapy, such as allopurinol
  • Patients are missing follow-up data
  • Hydrochlorothiazide and furosemide were used
  • Chronic kidney disease
Show all 14Show fewer
  • Oncolytic syndrome
  • Hemolytic anemia
  • Lead poisoning
  • Hyperparathyroidism
  • Hypothyroidism
  • A tyrosinase inhibitor was used
  • Patients with nonpancreatic primary tumors
  • Pregnant or postpartum women.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Wenbo Meng, M.D. Ph. D. contact

13919177177

mengwb@163.com

Zhengping An, M.D. contact

18298415512

anzhp2023@lzu.edu.cn

China1 site, 1 recruiting
  • Hepatopancreatobiliary Surgery Institute of Gansu Province

    Lanzhou, Gansu, 730000

    Wenbo Meng, MD,PhD, +8613919177177, mengwb@lzu.edu.cn

    Recruiting

Other trials in China

About this study

Official title: Whether Controlling Serum Uric Acid (SUA) Can Benefit Postoperative Survival in Patients With Pancreatic Cancer

This retrospective study aims to analyze the impact of postoperative changes in serum uric acid (SUA) levels on the prognosis of patients undergoing pancreatic cancer resection.

Read the detailed description

Serum uric acid is a risk factor for gallbladder cancer in men and has a strong effect on pancreatic cancer in women. It has also been shown that elevated intracellular serum uric acid can induce an inflammatory stress response, which may promote its transformation, while elevated extracellular serum uric acidy further stimulate tumor cell proliferation, migration, and survival, and promote the development of highly aggressive cancer. In this study, the changes of serum uric acid before and after surgery was used as a prognostic marker for the survival of pancreatic cancer patients.

Conditions
Serum Uric Acid
Being tested
serum uric acid test
Keywords
Serum uric acid, Pancreatic cancer, Pancreaticoduodenectomy, Distal pancreatectomy
Medical subject headings
Pancreatic Neoplasms

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • serum uric acid testDiagnostic test

    Detect the serum uric acid in blood sample

Study groups in NCT07091526
Study groupRoleWhat they receive
High serum uric acidThe increase of after serum uric acid operation compared with that before operation is≥10% Normal levels serum uric acid are typically 178 to 360 μm (3 to 6.8 mg/dl).
Receives: Diagnostic Test: serum uric acid test
Low serum uric acidThe increase of after serum uric acid operation compared with that before operation < 10% Normal serum uric acid levels are typically 178 to 360 μm (3 to 6.8 mg/dl).
Receives: Diagnostic Test: serum uric acid test

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Overall survival

    Overall survival was defined as the time from diagnosis to death.

    Measured: 3-5 years

Secondary outcomes (7)
  1. Recurrence-free survival

    Recurrence-free survival is the length of time from either the date of diagnosis or the start of therapy for a disease to the date of the first loco-regional or systemic recurrence.

    Measured: 3-5 years

  2. Cost of hospitalization

    The cost of the first hospitalization from admission to discharge.

    Measured: 3 months

  3. Length of hospital stay

    The first day of hospitalization for the first admission to the last day of discharge.

    Measured: 3 months

  4. Pancreatic fistula

    Whether or not pancreatic-intestinal anastomotic leakage occurred at the time of the first hospitalization.

    Measured: 3 months

  5. Biliary fistula

    Whether or not a biliary-intestinal anastomotic leak occurred at the time of the first hospitalization.

    Measured: 3 months

  6. Bleeding

    Whether or not there was bleeding after the first inpatient surgery.

    Measured: 3 months

  7. Abdominal cavity infection

    Whether or not there was an abdominal infection after the first inpatient surgery.

    Measured: 3 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted29 Jul 2025
  2. Study start29 Jul 2025
  3. Primary completion29 Dec 2026 (estimated)
  4. Study completion29 Dec 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Retrospective
Enrolment
168 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07091526
Sponsor's protocol ID
SUA-PC
Status last verified
Dec 2025
First submitted
21 Jul 2025
Last updated
19 Dec 2025
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Huang CF, Huang JJ, Mi NN, Lin YY, He QS, Lu YW, Yue P, Bai B, Zhang JD, Zhang C, Cai T, Fu WK, Gao L, Li X, Yuan JQ, Meng WB. Associations between serum uric acid and hepatobiliary-pancreatic cancer: A cohort study. World J Gastroenterol. 2020 Nov 28;26(44):7061-7075. doi: 10.3748/wjg.v26.i44.7061.

    PubMed 33311950
  • Fini MA, Elias A, Johnson RJ, Wright RM. Contribution of uric acid to cancer risk, recurrence, and mortality. Clin Transl Med. 2012 Aug 15;1(1):16. doi: 10.1186/2001-1326-1-16.

    PubMed 23369448

Questions about this trial

What is this clinical trial studying?

An observational study of Serum Uric Acid, run by Hepatopancreatobiliary Surgery Institute of Gansu Province at 1 site in China.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 14 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 19 Dec 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in China. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Wenbo Meng, M.D. Ph. D. (13919177177, mengwb@163.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Overall survival (time frame: 3-5 years). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT07091526, which also lists 2 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 19 Dec 2025.

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