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Fluoroscopic &Ultrasonographic Guidance of Superior Hypogastric Plexus Neurolysis in Intractable Pelvic Pain

The Role of Double Modality Fluoroscopic &Ultrasonographic Guidance of Superior Hypogastric Plexus Neurolysis in Treating Intractable Pelvic Cancer Pain: a Comparative Study.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03606811
Enrollment
60
Registered
2018-07-31
Start date
2018-08-05
Completion date
2019-08-15
Last updated
2020-01-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Intractable Pelvic Cancer Pain

Brief summary

fluoroscopic group & includes 30 patients where SHPB will be done Fluoroscopic-guided (the posterior oblique trajectory technique.the double modality group & includes 30 patients where SHPB will be done using our described new technique of performing the modified Mishra technique by injecting 3-5 ml of contrast media (lohexol=omnipaque) after getting the target position.

Interventions

PROCEDUREfluroscopic guided block

SHPB will be done Fluoroscopic-guided (the posterior oblique trajectory technique.

PROCEDUREdouble modality (ultrasound and fluroscopic) guided block

SHPB will be done using our described new technique of performing the modified Mishra technique by injecting 3-5 ml of contrast media (lohexol=omnipaque) after getting the target position. Then C-arm pictures will be checked (both P-A & dead lateral)

Sponsors

Assiut University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Age \> 18 years. * Intractable pelvic cancer pain (VAS \> 40 mm) * Pain is refractory to pharmacotherapy (both opioids and adjuvant therapy) or opioids' side effects are not tolerated.

Exclusion criteria

* Local or systemic sepsis. * Uncorrectable coagulopathy. * Neuropsychiatric illness. * History of drug abuse. * Pregnant or lactating patients. * Distorted local anatomy. * Patients who are known to be allergic to the used medications. * Cardiovascular or respiratory instability.

Design outcomes

Primary

MeasureTime frameDescription
pain relief will be assessed by VAS12 weekspain relief will be assessed by VAS (visual Analogue score) which is 100 mscale with left (0) end means no pain & right (10) end means the worst possible pain

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026