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Coeliac Plexus Neurolysis Versus Splanchnic Nerve Neurolysis


2022-12-01


2024-09-30


2025-03-31


100

Study Overview

Coeliac Plexus Neurolysis Versus Splanchnic Nerve Neurolysis

Pain is prevalent among patients with gastrointestinal cancers. Standard procedures such as coeliac plexus neurolysis (CPN) is effective in reducing pain, opioid requirement and related side effects for pancreatic cancer cases. Meanwhile, splanchnic nerve neurolysis (SNN) as an alternative to CPN is more effective for cancer pain relief. Although previous studies investigating the role of CPN/SNN mainly focus on pancreatic cancer cases, their efficacy on non-pancreatic abdominal cancer pain may not be accurately determined.

Pain is prevalent among patients with gastrointestinal cancers. There is abundant evidence that coeliac plexus neurolysis (CPN) is effective in reducing pain, opioid requirement and related side effects for pancreatic cancer cases while the evidence for other upper abdominal cancer pain is less robust but emerging. Meanwhile, there is an increasing interest in utilising splanchnic nerve neurolysis (SNN) as an alternative to CPN for cancer pain relief. Although previous studies investigating the role of CPN/SNN involved heterogenous types of intra-abdominal malignancies, majority of cases were pancreatic cancer. Therefore, their efficacy on non-pancreatic abdominal cancer pain may not be accurately determined.

  • Cancer Pain
  • OTHER: Coeliac plexus neurolysis
  • OTHER: Splanchnic nerve neurolysis
  • UW22-536

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates Results Reporting Dates Study Record Updates

2022-09-07  

N/A  

2023-11-29  

2022-09-12  

N/A  

2023-12-06  

2022-09-15  

N/A  

2023-11  

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

Design Details

Primary Purpose:
Treatment


Allocation:
Randomized


Interventional Model:
Parallel


Masking:
Triple


Arms and Interventions

Participant Group/ArmIntervention/Treatment
ACTIVE_COMPARATOR: Coeliac plexus neurolysis (CPN)

Coeliac plexus neurolysis (CPN) will be performed bilaterally. Neurolytic solution will be injected around the coeliac plexus (a network of nerves located in the abdomen).

OTHER: Coeliac plexus neurolysis

  • Coeliac plexus neurolysis (CPN) will be performed bilaterally. Neurolytic solution will be injected around the coeliac plexus (a network of nerves located in the abdomen).
EXPERIMENTAL: Splanchnic nerve neurolysis (SNN)

Splanchnic nerve neurolysis (SNN) will be performed bilaterally. Neurolytic solution will be injected around the splanchnic nerves (a nerve located at thoracic trunk).

OTHER: Splanchnic nerve neurolysis

  • Splanchnic nerve neurolysis (SNN) will be performed bilaterally. Neurolytic solution will be injected around the splanchnic nerves (a nerve located at thoracic trunk).
Primary Outcome MeasuresMeasure DescriptionTime Frame
pain scorePain intensity using numerical rating scale from 0 to 10 where 0 is no pain and 10 is the worst pain.at one week after procedure
Secondary Outcome MeasuresMeasure DescriptionTime Frame

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Name: Timmy CW Chan, MBBS

Phone Number: 22555791

Email: timmychancw@gmail.com

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person’s general health condition or prior treatments.

Ages Eligible for Study:
ALL

Sexes Eligible for Study:
18 Years

Accepts Healthy Volunteers:

    Inclusion Criteria:

  • Age>=18
  • Diagnosis of unresectable intra-abdominal cancer
  • Visceral pain attributable to the cancer with NRS >= 4
  • Able to understand instructions, give consent, complete questionnaires

  • Exclusion Criteria:

  • Primary pancreatic cancer or metastatic disease involving pancreas
  • Gross celiac axis distortion identified on imaging
  • Acute abdomen condition eg. Intraabdominal sepsis, tumor rupture
  • Other non-cancer causes attributable to the pain
  • Gross ascites
  • Previous coeliac plexus or splanchnic nerve neurolysis
  • Contraindications to neurolytic procedures eg. Bleeding tendency; local or systemic infections; allergic to local anesthetics, contrast or alcohol; intestinal obstruction; anatomical distortion along needle trajectory
  • Patients believed to be inappropriate for study by investigators

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

No publications available