Eligibility Module

Eligibility Module

The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.

Eligibility Module path is as follows:

Study -> Protocol Section -> Eligibility Module

Eligibility Module


Ignite Creation Date: 2025-12-25 @ 12:40 AM
Ignite Modification Date: 2025-12-25 @ 12:40 AM
NCT ID: NCT00388167
Eligibility Criteria: Inclusion Criteria: * Female and male with 18 years old at least. * Diagnosis of AI or CI. It will be based in Clinical History, signs and symptoms that the patient takes, discovery of studies of radiology and results of cultivation and/or studies of anatomopathology positives for Candida spp. or Aspergillus spp. * Patients with AI, must be refractory to or intolerant of other therapies antifungal used in the hospital. * Patients with CI, must be or not refractory to or intolerant of other therapies antifungal used in the hospital. Exclusion Criteria: * Patients with diagnosis uncertain based in one or more of next criterions: Cultivation positive for Candida in an only localization (urine, spittle, end/current of catheter; osteomyelitis or endocarditis by Candida without treatment appropriated surgical; infection by Candida of prosthetic material without retired of the same; positive blood cultive for Candida in appearance of vascular prosthesis; allergic lung Aspergillosis; and aspergilloma or aspergillosis eye without treatment appropriated surgical). * Allergic / hypersensitivity to caspofungin. * Insufficiency several liver (rate of Chile-Pugh \>9). * Prediction of survival \<5 days. * Pregnant or breast feeding. * Previous Participation of patient in this study. * Presence of other disease or any condition that it can mix up the interpretation of results or create risks. * Previous Participation of patient in other clinical study that it involve the administration of a drug in investigation in the 14 days previous to your inclusion in the study or during the administration of caspofungin. We can include patients took with antineoplastic drugs in research whenever at lefts a Investigator Coordinator authorizes it before
Healthy Volunteers: False
Sex: ALL
Minimum Age: 18 Years
Study: NCT00388167
Study Brief:
Protocol Section: NCT00388167