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Recruiting NCT07333612

IM Bands in Inactive Hepatic CE

Observational Cystic 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
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Cystic Echinococcosis. Basic parameters: from 18 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
Italy
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Comparison of Immunoblotting Bands Pattern in Patients With Treated Versus Untreated Inactive Echinococcal Cysts of the Liver

Overview

Comparison of immunoblotting bands pattern in patients with treated versus untreated echinococcal cysts of the liver

Primary outcome measures

  • Percentage of patients with spontaneously inactivated hepatic CE cysts with positive WB and RT t differente times from diagnosis. [Time frame: from September 2024 to September 2026]
Secondary outcome measures (2)
  • Percentage of cysts that remaine inactive after treatment or reactivate [Time frame: from september 2024 to September 2026]
  • Percentage of patients with inactivated cysts after treatment with positive WB results at different time point from the first observation of an inactive stage. [Time frame: from September 2024 to September 2026]

Eligibility criteria

Inclusion criteria

  • Only Hepatic echinococcal cysts
  • Age > 18 years
  • At leat 2 clinical evaluation

Exclusion criteria

  • different location of echinococcal cysts
  • Age < 18 years --less then 2 clinical evalutation

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

Italy · 1 center
  • Fondazione IRCCS Policlinico San Matteo di Pavia — Pavia

Identifiers

NCT: NCT07333612 · 08075323

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗