Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
40 participants
OBSERVATIONAL
1999-05-31
2000-04-30
Brief Summary
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Detailed Description
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Conditions
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Keywords
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Study Design
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CASE_CONTROL
PROSPECTIVE
Study Groups
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1
Response to medical treatment
No interventions assigned to this group
2
Failure to medical treatment (surgery or percutaneous resolution)
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
2. Both genders
3. Older 15 years
Exclusion Criteria
2. Positive hemoculture
3. Negative ELISA for amoebic antigens
4. Immunosupresion (HIV)
5. Abdominal or biliary surgery antecedents
6. Abdominal neoplasia antecedents
16 Years
80 Years
ALL
No
Sponsors
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Universidad Nacional Autonoma de Mexico
OTHER
Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran
OTHER
Hospital Central "Dr. Ignacio Morones Prieto"
OTHER
Universidad Autonoma de San Luis Potosí
OTHER
Responsible Party
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Epidemiologia Clinica, Universidad Autonoma de San Luis Potosí
Principal Investigators
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Martín Sánchez-Aguilar 1, MSc
Role: PRINCIPAL_INVESTIGATOR
1. Department of Experimental Surgery, Faculty of Medicine, Universidad Autónoma de San Luis Potosí
Onofre Morán-Mendoza, PhD
Role: STUDY_DIRECTOR
Department of Clinical Epidemiology, Faculty of Medicine, Universidad Autónoma de San Luis Potosí
Locations
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Department of Surgery, Instituto Nacional de Ciencias Médicas y Nutrición "Salvador Zubirán".
Mexico City, Mexico DF, Mexico
Faculty of Medicine, Universidad Autónoma de San Luis Potosí
San Luis Potosí City, San Luis Potosí, Mexico
Countries
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Other Identifiers
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PFP-ALA
Identifier Type: -
Identifier Source: org_study_id