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 @ 4:31 PM
Ignite Modification Date:
2025-12-24 @ 4:31 PM
NCT ID:
NCT01681966
Eligibility Criteria:
Inclusion Criteria:
* Male subjects between 18-70 years of age who are scheduled to undergo open one sided herniorrhaphy surgery;
* Subjects have a BMI of less than 30 kg/m2;
* Subjects are in good physical health (other than the need for the surgical procedure) as judged by physical and laboratory examinations and have a negative urine based screen for drugs of abuse;
* Subjects must agree to refrain from ingesting any analgesic medication for at least 2 days (or 5 half-lives of the analgesic drug) prior to surgery; refrain from alcohol and excessive caffeine intake on the day of surgery and during 72 hours after surgery;
* Subject must be capable of reading, comprehending, and signing the informed consent form;
Exclusion Criteria:
* Subjects with a history of melena or any significant hepatic, renal, endocrine, cardiac, neurological, psychiatric, gastrointestinal, pulmonary, hematologic, or metabolic disorders;
* Subjects with a history of any type of cancer within 5 years of surgery;
* Subjects with any history of alcohol or substance abuse;
* Subjects that have a history of uncontrolled hypertension;
* Subjects with a known hypersensitivity to any local anesthetic drug;
* Subjects with a hemoglobin concentration of less than 10.0 g/dL;
* Subjects with any clinically significant abnormal lab result (as judged by the Principal Investigator);
* Subjects with atrial fibrillation/flutter, an inserted pacemaker, or complete left bundle branch block (LBBB) on ECG; or myocardial infarction within 6 months prior to surgery;
* Subjects with a clinically significant abnormal ECG at screening;
* Subjects with any condition or history judged by the Investigator to place the subject at increased risk;
* Subjects judged by the Investigator to be unable or unwilling to comply with the requirements of the protocol;
* Subjects who have used an investigational drug within 30 days prior to entering the study;
* Subjects who have donated blood within 3 months prior to the start of the study;
* Subjects who are members of the study site staff directly involved with the study or a relative of the Sponsor or other personnel involved with the study;
Healthy Volunteers:
False
Sex:
MALE
Minimum Age:
18 Years
Study:
NCT01681966
Study Brief:
Protocol Section:
NCT01681966