- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07333612
IM Bands in Inactive Hepatic CE
December 30, 2025 updated by: Raffaella Lissandrin, Fondazione IRCCS Policlinico San Matteo di Pavia
Comparison of Immunoblotting Bands Pattern in Patients With Treated Versus Untreated Inactive Echinococcal Cysts of the Liver
Comparison of immunoblotting bands pattern in patients with treated versus untreated echinococcal cysts of the liver
Study Overview
Status
Recruiting
Conditions
Study Type
Observational
Enrollment (Estimated)
100
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
PV
-
Pavia, PV, Italy, 27100
- Recruiting
- Fondazione IRCCS Policlinico San Matteo di Pavia
-
Contact:
- Raffaella Lissandrin
- Phone Number: 3355853501
- Email: r.lissandrin@smatteo.pv.it
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
patients affected by cystic echinococcosis of the liver.
Description
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
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
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
|
from 0 to 100%
|
from September 2024 to September 2026
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Percentage of cysts that remaine inactive after treatment or reactivate
Time Frame: from september 2024 to September 2026
|
from 0 to 100%
|
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
|
from 0 to 100%
|
from September 2024 to September 2026
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
September 23, 2025
Primary Completion (Estimated)
May 1, 2026
Study Completion (Estimated)
September 1, 2026
Study Registration Dates
First Submitted
December 30, 2025
First Submitted That Met QC Criteria
December 30, 2025
First Posted (Estimated)
January 12, 2026
Study Record Updates
Last Update Posted (Estimated)
January 12, 2026
Last Update Submitted That Met QC Criteria
December 30, 2025
Last Verified
December 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 08075323
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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