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NCT05869474Recruiting

Implantation of iodine125-Seeds Combined With Chemotherapy in the Treatment of Metastatic Pancreatic Carcinoma

Endoscopic Ultrasound-guided Intratumoral Iodine125-Seeds Implantation Combined With Gem/Nab-P Chemotherapy Versus Gem/Nab-P Alone for Metastatic Pancreatic Carcinoma: a Randomized, Controlled, Trial

Source: ClinicalTrials.gov · Last updated 4 Aug 2023 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

The goal of this clinical trial is to evaluate the clinical efficacy and safety of endoscopic ultrasonography (EUS)-guided radioactive iodine 125 seeds in combination with AG regimen chemotherapy for the treatment of metastatic pancreatic cancer. The main questions it aims to answer are: * whether the combination of minimally invasive endoscopy-guided local radiation therapy with chemotherapy may improve overall survival * the adverse events of the combination therapy Participants will receive the implantation of radioactive seeds under EUS guide. 48h after implantation, chemotherapy with Gem/nab-P given on days 1 and 8 of each 21-day cycle will be conducted. Researchers will compare the I125+AG group with the group that takes AG chemotherapy alone to see if the overall survival can be improved.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
206 (estimated)
First submitted
11 May 2023
Start date
1 Aug 2023
Primary completion date
Dec 2027
Lead sponsor
Changhai Hospital
NCT number
NCT05869474

What you commit to

  • Study type: Interventional
  • Planned participants: 206
  • From 1 Aug 2023 to the primary completion date, Dec 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Contraindication of EUS-guide procedure or technical infeasibility (e.g.,coagulation disorder, anatomical changes, large vessels along the puncture path)
  • Presence of deep vein thrombosis or pulmonary embolism
  • Presence of HIV, HBV, HCV infection or other uncontrollable active infection
  • Hypersensitivity to chemotherapy drugs
  • History of other malignancies within 5 years
  • Peripheral neuropathy or interstitial lung disease within 5 years

Other

  • Pregnant or breastfeeding
  • Presence of brain metastases
  • Patient is enrolled in any other clinical protocol or investigational trial.

Who the study is looking for

  • (Before the trial, subjects must meet all of the requirements listed below in order to be enrolled)
  • 18 to 80 years old;
  • Stage IV pancreatic ductal adenocarcinoma with distant metastases confirmed by clinical, imaging, and pathology, and the primary and metastatic mass can be measured on imaging.
  • No treatment history of chemotherapy, radiotherapy, or surgery
  • Expected survival \> 6 months
  • ECGO score of 0-2
  • Eligible for chemotherapy (white blood cell \> 3.5×109/L, neutrophil value \> 1.5×109/L, hemoglobin \> 80g/L, platelets \> 100×109/L, albumin \> 25g/L, alanine aminotransferase or aspartate aminotransferase ≤ 3 times the upper limit of normal and total bilirubin level ≤ 34.2umol/L, creatinine \< 176.8 umol/L, normal ECG)
  • Signed written informed consent;

Age in the registry: 18 years to 80 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Changhai Hospital
Coordinator of this site? Confirm its status
ShanghaiChinaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.