Recruiting NCT06316154
Presentation of Protoscolexes and Acephalocysts in the Fibrous Capsule Area of the Liver With Echinococcosis
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Echinococcectomy.
- Who it may be relevant to
- Registry conditions: Echinococcosis, Hepatic. Basic parameters: 18 years — 80 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Uzbekistan
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Presentation of Protoscolexes and Acephalocysts in the Fibrous Capsule Area of the Liver With Echinococcosis During Organ-preserving Surgery
Overview
The objective of the study is to determine the presence of germinal elements of echinococcosis in the liver parenchyma next to and in the thickness of the fibrous capsule of hydatid cysts.
Interventions
- Procedure Echinococcectomy
Echinococcectomy with subsequent pathomorphological analysis of liver parenchyma next to and in the thickness of the fibrous capsule
Primary outcome measures
- Presence of viable germinal elements of echinococcosis [Time frame: 1 day]
Secondary outcome measures (1)
- Recurrence of liver echinococcosis [Time frame: 1 year]
Eligibility criteria
Inclusion criteria
- Presence of primary or recurrent liver echinococcosis disease requiring surgical treatment
- Cyst diametr >5 cm;
- Performing one of the surgical treatment of liver echinococcosis with intraoperative sampling of part of the fibrous capsule with or without adjacent liver tissue for research;
- Signed informed consent of patients for inclusion in the study;
Exclusion criteria
- Liver echinococcosis with cysts less than 5 cm in diametr;
- Presence of severe concomitant disorders
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Cohort
Study locations
Uzbekistan · 1 center
- Republican specialized scientific and practical medical center of surgery named after acad — Tashkent
Identifiers
NCT: NCT06316154 · 12032024