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Percutaneous Translumbar Vs Transhepatic Permcath

Percutaneous Translumbar Vs Transhepatic Insertion of Long Term Hemodialysis Catheters (Permcath) After Failure of Classic Accesses

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05666375
Enrollment
52
Registered
2022-12-27
Start date
2023-01-01
Completion date
2026-01-01
Last updated
2022-12-27

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

Conditions

End Stage Renal Disease

Brief summary

The aim of the study is to emphasize the technique , success rate , efficacy of translumbar and transhepatic approaches and shed light on the complications of both methods and through comparison we can give recommendations to either of these methods.

Detailed description

For selected ESRD patients who have exhausted all conventional access routes , translumbar and transhepatic permcath provide additional sites for access. This study will compare the two methods in terms of technical success (position of catheter tip), patency (primary defined as the number of catheter days from initial placement until removal & secondary defined as the number of catheter days after device replacement using the same access site) , mean cumulative duration of catheter in situ defined as the cumulative catheter days divided by the number of patients, function (adequacy of dialysis based on Urea Reduction Ratio URR & Simplified Daugirdas Formula Kt/V) and complications (infectious; exit site infection & sepsis and non-infectious; thrombosis, catheter migration, hematoma, intraperitoneal hemorrhage.

Interventions

PROCEDUREPercutaneous translumbar and transhepatic permcath

For selected ESRD patients who have exhausted all conventional access routes , translumbar and transhepatic insertion of long term hemodialysis catheters provide additional sites for access

Sponsors

Assiut University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

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

Inclusion criteria

\- Chronic dialysis patients with failed classic routes of catheterization ( internal jugular, subclavian and femoral veins bilaterally ) as well as non-functioning a-v fistulas.

Exclusion criteria

1. Patients with uncorrectable coagulopathy. 2. Patients on long term anticoagulants 3. Concurrent active infection. 4. Sgnificant abdominal ascites. (transhepatic) 5. Cirrhotic liver disease patients. (transhepatic) 6. Morbid obesity. (translumbar)

Design outcomes

Primary

MeasureTime frameDescription
Catheter patencyBaselinepatency (primary defined as the number of catheter days from initial placement until removal & secondary defined as the number of catheter days after device replacement using the same access site) , mean cumulative duration of catheter in situ defined as the cumulative catheter days divided by the number of patients

Contacts

Primary ContactAbdallah Morsy
Abdallahmorsynah96@gmail.com+2001093744274
Backup ContactHany Seif
Hanyseifrad@yahoo.com+2001005618665

Outcome results

None listed

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