Actively Recruiting
Hypogastric Plexus Block and Ganglion Impar Block for Cervical and Endometrial Cancer Pain Management
Led by University of Brawijaya · Updated on 2025-07-10
36
Participants Needed
1
Research Sites
79 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This study compared the efficacy and safety of superior hypogastric plexus block and ganglion impar block procedures on the management of pelvic and perineal cancer pain in patients with cervical and endometrial cancer
CONDITIONS
Official Title
Hypogastric Plexus Block and Ganglion Impar Block for Cervical and Endometrial Cancer Pain Management
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Unbearable cancer pain resistant to WHO pain ladder medication for at least 2 weeks
- Tired of taking oral medication or experiencing complications such as respiratory depression, nausea, vomiting, opioid-induced constipation, or gastrointestinal disturbances
- Diagnosed with pelvic floor pain by a FIPP-certified pain specialist
- Diagnosed with perineal pain by a FIPP-certified pain specialist
- Numerical Rating Scale pain score greater than 4
- Female aged over 18 years
- Able and willing to provide informed consent
You will not qualify if you...
- Refusal to participate in the research
- Blood clotting disorders, including use of anticoagulant drugs
- Local infection in the area where the procedure would be performed
- Loss to follow-up
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
General Hospital Saiful Anwar Malang
Malang, East Java, Indonesia, 65111
Actively Recruiting
Research Team
R
Ristiawan M Laksono, MD,FIPP
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
TRIPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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