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: 2025-12-24 @ 4:27 PM
Ignite Modification Date: 2025-12-24 @ 4:27 PM
NCT ID: NCT03599466
Eligibility Criteria: Inclusion Criteria: * Male and non-pregnant female, 18 to 55 years of age * Body Mass Index between 18 to 30 kg/m2 * Accessible vein for blood sampling * High probability for compliance and completion of the study * Female subjects must agree to practice abstinence or take effective contraceptive methods to prevent pregnancy from the start of the screening and until two weeks of last dose administration. Exclusion Criteria: * Clinically significant hepatic, renal, biliary, cardiovascular, gastrointestinal, haematological and other chronic and acute diseases within 3 months prior to the study * Clinically significant abnormality in physical examination, vital sign, laboratory test results, ECG evaluation, urine test, blood chemistry or haematological test * Regular consumption of tobacco used in any forms * Regular consumer of alcohol (more than one drink per day) * Blood donation within 4 weeks prior to the start of the study * Use of lisinopril within 4 weeks before the study * Use of antihypertensive medications or angiotensin-converting enzyme (ACE) inhibitors within 4 weeks before the study * Volunteer in any other clinical drug study within 2 months prior to this study * Hypersensitivity to lisinopril or other drugs in its class * History of drug abuse in any form * Female subjects who are breastfeeding or pregnant
Healthy Volunteers: True
Sex: ALL
Minimum Age: 18 Years
Maximum Age: 55 Years
Study: NCT03599466
Study Brief:
Protocol Section: NCT03599466