Coeliac Plexus vs Splanchnic Nerve Neurolysis for Upper Abdominal Cancer Pain

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorBangladesh Medical University

About this trial

The goal of this clinical trial is to determine whether Neurolytic Splanchnic Nerve Block (NSNB) reduces pain in adults with upper abdominal malignancies. It will also evaluate the safety of Neurolytic Splanchnic Nerve Block (NSNB). The main questions it aims to answer are:

Does NSNB reduce pain intensity compared to Neurolytic Coeliac Plexus Block (NCPB), as measured by the Visual Analog Scale (VAS)? What adverse effects do participants experience when receiving Neurolytic Splanchnic Nerve Block (NSNB)?

Investigators will compare Neurolytic Splanchnic Nerve Block (NSNB) with Neurolytic Coeliac Plexus Block (NCPB) to determine which intervention provides more effective and safer pain relief.

Participants will:

* receive either NSNB or NCPB under fluoroscopic guidance * be monitored immediately and for 2 hours after the procedure for any complications Have their pain intensity recorded immediately after the procedure, and at 7 days, 1 month, and 3 months * be evaluated for quality-of-life using European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire - Core 3 (EORTC QLQ-C30) at 1 month and 3 months. * have their opioid consumption tracked throughout the study.

Eligibility criteria

Qualifiers

Adult patient

Both genders

Diagnosed case of upper abdominal malignancy (pancreatic, gastric, hepatic, or biliary origin)

Experiencing moderate to severe pain (≥5 on a 10 point visual analog scale)

Disqualifiers

Previous coeliac plexus block, splanchnic nerve block, or major abdominal nerve ablation

Severe spinal deformities or anatomical distortion at the coeliac plexus or splanchnic nerve site

Local or systemic infection at or near the block site

Known allergy to local anesthetics or neurolytic agents

Trial design

Treatments tested in this trial

  • Neurolytic Coeliac Plexus Block (NCPB)
  • Neurolytic Splanchnic Nerve Block (NSNB)

Treatment groups

44 Participants
are divided into 2 treatment groups

Sponsors and collaborators