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Terminated Phase 2 Interventional Results available

High or Standard Intensity Radiation Therapy After Gemcitabine Hydrochloride and Nab-paclitaxel in Treating Patients With Pancreatic Cancer That Cannot Be Removed by Surgery

ClinicalTrials.gov ID: NCT01921751

Public ClinicalTrials.gov record NCT01921751. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 22, 2026, 4:37 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase II Randomized Trial Evaluating the Addition of High or Standard Intensity Radiation to Gemcitabine and Nab-paclitaxel for Locally Advanced Pancreatic Cancer

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This randomized phase II trial studies how well high or standard intensity radiochemotherapy after gemcitabine hydrochloride and paclitaxel albumin-stabilized nanoparticle formulation (nab-paclitaxel) work compared with gemcitabine hydrochloride and nab-paclitaxel alone in treating patients with pancreatic cancer that cannot be removed by surgery. Drugs used in chemotherapy, such as gemcitabine hydrochloride and nab-paclitaxel, work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing or by stopping them from spreading. Radiation therapy uses high-energy x-rays to kill tumor cells. Drugs, such as capecitabine, may make tumor cells more sensitive to radiation therapy. Giving radiation therapy in different ways and adding chemotherapy may kill more tumor cells. It is not yet known whether high intensity radiochemotherapy after gemcitabine hydrochloride and nab-paclitaxel is more effective than standard intensity radiochemotherapy after gemcitabine hydrochloride and nab-paclitaxel or gemcitabine hydrochloride and nab-paclitaxel alone in treating pancreatic cancer.

Study identification

NCT ID
NCT01921751
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Enrollment
20 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Aug 2013 (Type not available)
Primary completion
Jun 2016 (Actual)
Completion
Jun 2016 (Actual)
Last update posted
Jul 13, 2018

2013 – 2016

United States locations

U.S. sites
46
U.S. states
23
U.S. cities
42
Facility City State ZIP Site status
Kaiser Permanente Oakland-Broadway Oakland California 94611 —
Kaiser Permanente Medical Center - Santa Clara Santa Clara California 95051 —
Kaiser Permanente Cancer Treatment Center South San Francisco California 94080 —
Emory University/Winship Cancer Institute Atlanta Georgia 30322 —
Saint Joseph Hospital Chicago Illinois 60657 —
Decatur Memorial Hospital Decatur Illinois 62526 —
OSF Saint Francis Medical Center Radiation Oncology Service at the Central Illinois Comprehensive CC Peoria Illinois 61615-7827 —
OSF Saint Francis Medical Center Peoria Illinois 61637 —
Radiation Oncology Associates PC Fort Wayne Indiana 46804 —
Parkview Hospital Randallia Fort Wayne Indiana 46805 —
McFarland Clinic PC-William R Bliss Cancer Center Ames Iowa 50010 —
Iowa Methodist Medical Center Des Moines Iowa 50309 —
Ochsner Medical Center Jefferson New Orleans Louisiana 70121 —
Johns Hopkins University/Sidney Kimmel Cancer Center Baltimore Maryland 21287 —
Boston Medical Center Boston Massachusetts 02118 —
Saint Joseph Mercy Hospital Ann Arbor Michigan 48106-0995 —
Sanford Clinic North-Bemidgi Bemidji Minnesota 56601 —
Mayo Clinic Rochester Minnesota 55905 —
Rice Memorial Hospital Willmar Minnesota 56201 —
Mercy Hospital Springfield Springfield Missouri 65804 —
CoxHealth South Hospital Springfield Missouri 65807 —
Mercy Hospital Saint Louis St Louis Missouri 63141 —
Fox Chase Cancer Center at Virtua Memorial Hospital of Burlington County Mount Holly New Jersey 08060 —
Capital Health Medical Center-Hopewell Pennington New Jersey 08534 —
University of Rochester Rochester New York 14642 —
Sanford Bismarck Medical Center Bismarck North Dakota 58501 —
Roger Maris Cancer Center Fargo North Dakota 58122 —
Akron General Medical Center Akron Ohio 44307 —
Bryn Mawr Hospital Bryn Mawr Pennsylvania 19010 —
Paoli Memorial Hospital Paoli Pennsylvania 19301 —
University of Pennsylvania/Abramson Cancer Center Philadelphia Pennsylvania 19104 —
Reading Hospital West Reading Pennsylvania 19611 —
Lankenau Medical Center Wynnewood Pennsylvania 19096 —
Rhode Island Hospital Providence Rhode Island 02903 —
Sanford USD Medical Center - Sioux Falls Sioux Falls South Dakota 57117-5134 —
Thompson Cancer Survival Center Knoxville Tennessee 37916 —
M D Anderson Cancer Center Houston Texas 77030 —
Intermountain Medical Center Murray Utah 84157 —
McKay-Dee Hospital Center Ogden Utah 84403 —
Huntsman Cancer Institute/University of Utah Salt Lake City Utah 84112 —
Central Vermont Medical Center/National Life Cancer Treatment Berlin Corners Vermont 05602 —
University of Vermont Medical Center Burlington Vermont 05401 —
Saint Vincent Hospital Green Bay Wisconsin 54301 —
Saint Mary's Hospital Green Bay Wisconsin 54303 —
Bay Area Medical Center Marinette Wisconsin 54143 —
Door County Cancer Center Sturgeon Bay Wisconsin 54235-1495 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01921751, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 13, 2018 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01921751 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →