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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT02220062
Other study ID # 2014-02-088-005
Secondary ID
Status Not yet recruiting
Phase N/A
First received July 21, 2014
Last updated August 18, 2014
Start date August 2014

Study information

Verified date August 2014
Source Samsung Medical Center
Contact n/a
Is FDA regulated No
Health authority South Korea: Institutional Review Board
Study type Interventional

Clinical Trial Summary

Pancreatic cancer related pain can be difficult to control, even with high doses of narcotics, whose adverse effects may further impair quality of life. So EUS-CPN(endoscopic ultrasound guided celiac plexus neurolysis) is well established as an effective technique for controlling pain and reducing narcotic requirements in patients with pancreatic cancer. Recently, celiac ganglia can be visualized and accessed by endoscopic ultrasound. So it allows for direct injection into individual celiac ganglia to perform celiac ganglia neurolysis. This more precise delivery of therapeutic drug will offers the potential for enhanced efficacy and safety. To evaluate this hypothesis, this randomized controlled trial aimed to compare the efficacy and safety of EUS-CGN(Endoscopic ultrasound guided celiac ganglia neurolysis) vs. Bilateral EUS-CPN(Endoscopic ultrasound guided celiac plexus neurolysis) in providing relief from pancreas cancer-related pain.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 166
Est. completion date
Est. primary completion date August 2016
Accepts healthy volunteers No
Gender Both
Age group 19 Years and older
Eligibility Inclusion Criteria:

1. At least 19 years old age (above 70 years old age, need the consent of the legal representative)

2. Inoperable pancreatic cancer patients

3. Pancreatic cancer patients with inadequate pain control by pain killer (VAS score 4 points or more)

4. Patient who agree to participate in this study

Exclusion Criteria:

1. Abnormal clotting (international normalized ratio =1.5)

2. Reduced platelet count (=50000/µL)

3. Use of anticoagulation agents

4. Presence of gastric and/or esophageal varices

5. Anatomical deformity due to past surgery

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Procedure:
EUS-CPN
After initially identifying the celiac trunk on endoscopic ultrasound, each injection of 5~10cc ethanol would be performed as bilateral injections at the celiac trunk.
EUS-CGN
First, identify celiac ganglia. If the celiac ganglia are visualized under linear EUS, the injection of 2~3cc ethanol are applied directly into the each ganglia. If the ganglia are not identified by EUS, bilateral EUS-CPN would be performed

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Samsung Medical Center

Outcome

Type Measure Description Time frame Safety issue
Primary percentage of participants with 50% decrease or less than 3 points in Pain Visual Analogue Scale (VAS) 1 week after procedure No
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