- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05010811
Two Cases of Pulmonary Cysticercosis Manifesting as Pleural Effusion: Case Report and Literature Review
August 24, 2021 updated by: Second Affiliated Hospital, School of Medicine, Zhejiang University
Isolation lung cysticercosis reports are rare in literature.
Most lung lesions were characterized by nodules.
The investigators access one case which was characterized with pulmonary cavity and pleural effusion by Gupta N, et al in 2015 from PUBMED and Medline.
But pleural effusion and exudative lesions is reported for the first time.
Study Overview
Status
Completed
Conditions
Detailed Description
Cysticercosis is an important public health problem in developing countries.
The major involvement sites are the central nervous system and the eyes,although striated muscles and subcutaneous tissues are frequently involved in the disseminated form of disease.
Pulmonary involvement in cysticercosis is very rare and ill-defined nodular shadows distributed throughout the lung is the usual radiological presentation.
Only one case of cysticercosis presenting as lung cavity with pleural effusion has been reported so far in literature.
The investigators describe two cases in which pleural effusion due to cysticercosis were detected on X and CT.
Study Type
Observational
Enrollment (Actual)
2
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
45 years to 67 years (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Two patients with pleural effusion presenting with chest tightness and chest pain were enrolled in this study with a definitive diagnosis of cysticercosis confirmed by pleural effusion examination
Description
Inclusion Criteria:
- Clinical diagnosis of Pulmonary Cysticercosis。
- With pleural effusion
Exclusion Criteria:
1.No cysticercosis was found by biopsy or antibody test
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 |
---|---|---|
Amount of pleural effusion
Time Frame: 9 months
|
cm
|
9 months
|
Rate of Eosinophil ratio
Time Frame: 9 months
|
Percentage(%)
|
9 months
|
Changes of lesions under chest radiography or CT
Time Frame: 9 months
|
no change, change, complete absorption
|
9 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Study Director: Pingli Wang, MD, the same research center
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)
October 22, 2016
Primary Completion (ACTUAL)
January 18, 2017
Study Completion (ACTUAL)
April 28, 2017
Study Registration Dates
First Submitted
July 11, 2021
First Submitted That Met QC Criteria
August 15, 2021
First Posted (ACTUAL)
August 18, 2021
Study Record Updates
Last Update Posted (ACTUAL)
August 30, 2021
Last Update Submitted That Met QC Criteria
August 24, 2021
Last Verified
September 1, 2016
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
- Central Nervous System Diseases
- Nervous System Diseases
- Infections
- Respiratory Tract Diseases
- Pleural Diseases
- Central Nervous System Infections
- Parasitic Diseases
- Helminthiasis
- Cestode Infections
- Central Nervous System Helminthiasis
- Central Nervous System Parasitic Infections
- Pleural Effusion
- Cysticercosis
- Taeniasis
- Neurocysticercosis
Other Study ID Numbers
- 2016-122
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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