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Search / Trial NCT06978673

Neurolytic Block Techniques In Abdominal Visceral Cancer Pain

Launched by INSTITUTO DO CANCER DO ESTADO DE SÃO PAULO · May 16, 2025

Trial Information

Current as of June 26, 2025

Not yet recruiting

Keywords

Cancer Pain Visceral Pain Abdominal Cancer Cancer Abdominal Pain Cancer Related Pain Pain Management Neurolytic Block Splanchnic Nerve Block Celiac Plexus Block Sympathetic Neurolysis

ClinConnect Summary

This clinical trial is studying two different techniques to help manage severe abdominal pain in patients with cancer. The researchers want to see which technique—celiac plexus neurolysis or splanchnic nerve neurolysis—works better for relieving visceral pain that comes from specific types of abdominal cancers, like those affecting the stomach, liver, or pancreas. They are also looking at how these treatments impact the overall quality of life for patients.

To participate in this study, you need to be at least 18 years old and have persistent abdominal pain related to your cancer that hasn’t improved with strong pain medications. You should also be experiencing side effects from these medications that are hard to manage. However, certain health conditions, like liver or kidney failure, or taking blood-thinning medications, would make you ineligible for the trial. If you join, you can expect to receive one of the two treatment techniques and be monitored to see how well it helps with your pain and overall well-being. This study is not yet recruiting participants, so there will be more information available soon for those interested.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Patients aged 18 years or older Presence of localized visceral pain in the upper abdomen originating from cancer of the stomach, duodenum, distal esophagus, ascending or transverse colon, liver, biliary tract, or pancreas
  • Ineffectiveness of analgesic treatment with third-step opioids according to the WHO analgesic ladder, including:
  • Opioids (≥ 60 mg/day of morphine equivalents) Antidepressants (tricyclic or dual-action), at any dosage Gabapentinoids, at any dosage Presence of side effects from analgesics that are difficult to manage with medication
  • Exclusion Criteria:
  • Presence of ascites Presence of deep vein thrombosis Presence of hepatic failure: Child-Pugh class B or C Presence of renal failure: estimated glomerular filtration rate (eGFR) \< 60 ml/min/1.73 m² Use of any anticoagulant medication
  • Clinical coagulation disorder, defined as:
  • INR \> 1.5 Prothrombin activity \< 70% or prothrombin time \> 13.5 seconds aPTT \> 40 seconds Cardiovascular failure: NYHA class III

About Instituto Do Cancer Do Estado De São Paulo

The Instituto do Câncer do Estado de São Paulo (ICESP) is a leading cancer research and treatment institution in Brazil, dedicated to advancing the understanding and management of cancer through innovative clinical trials and comprehensive patient care. As a prominent sponsor of clinical trials, ICESP focuses on developing cutting-edge therapies and improving treatment outcomes for cancer patients. With a commitment to scientific excellence and collaboration, the institute plays a pivotal role in contributing to national and international cancer research initiatives, ultimately striving to enhance the quality of life for individuals affected by cancer.

Locations

São Paulo, Sp, Brazil

Patients applied

0 patients applied

Trial Officials

Angela M Sousa, MD. PhD.

Study Director

Instituto do Cancer do Estado de São Paulo

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported