Actively Recruiting

Phase 2
Age: 18Years - 90Years
All Genders
NCT03498326

Gemcitabine and Celecoxib Combination Therapy in Treating Patients With R0 Resection Pancreatic Cancer

Led by Second Affiliated Hospital, School of Medicine, Zhejiang University · Updated on 2018-05-30

480

Participants Needed

1

Research Sites

625 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The prognosis of pancreatic cancer is extremely poor, even in those patients who had underwent surgery, the 5-year survival is still less than 10%. Current guidelines recommend Gemcitabine monotherapy for R0 resection of pancreatic cancer. Inflammation plays an critical role in the development and progression of pancreatic cancer. Here we intend to assess the synergistic effect of using celecoxib in combination with gemcitabine on the treatment of R0 resection of pancreatic cancer.

CONDITIONS

Official Title

Gemcitabine and Celecoxib Combination Therapy in Treating Patients With R0 Resection Pancreatic Cancer

Who Can Participate

Age: 18Years - 90Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • 18 years old and above
  • Surgery for R0 resection
  • No prior gemcitabine chemotherapy for other malignancies
  • Eastern Cooperative Oncology Group score between 0 and 2
  • Neutrophil count at least 1.5 x 10^9/ml, platelet count at least 100 x 10^9/ml, hemoglobin at least 80 g/L
  • Liver function: bilirubin ≤ 1.5 times upper limit of normal; alanine aminotransferase and aspartate aminotransferase ≤ 3 times upper limit
  • Kidney function: creatinine ≤ 1.2 mg/dL
Not Eligible

You will not qualify if you...

  • Endocrine carcinoma, acinar pancreatic carcinoma, or cystadenocarcinoma
  • Surgery for pancreatic cancer not meeting R0 resection criteria
  • Prior radiotherapy for pancreatic cancer before surgery
  • Malignant brain metastases
  • History of other serious cancers
  • Active infection or severe diarrhea
  • Allergy or intolerance to celecoxib or related drugs such as aspirin or NSAIDs
  • Pregnancy or breastfeeding
  • Active gastrointestinal ulcer, hemorrhage, or perforation
  • Severe mental illness
  • Severe heart failure
  • History of serious cardiovascular thrombotic events
  • Severe hypertension

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 1 location

1

the second affiliated hospital of Zhejiang University

Hangzhou, Zhejiang, China, 310009

Actively Recruiting

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Research Team

T

Tingbo Liang

CONTACT

X

Xueli Bai

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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