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 @ 12:43 AM
Ignite Modification Date:
2025-12-25 @ 12:43 AM
NCT ID:
NCT00154167
Eligibility Criteria:
Inclusion Criteria:
* Between 10-65 years of age
* Body weight between 35 to 110 kg
* Healthy as determined by the Investigator based on medical history, physical examination, and 12 Lead ECG
* Clinical laboratory tests within the reference ranges or within clinically acceptable limits according to the Investigator
* Normal lip, nose, chin, and tongue sensations
* Women of childbearing potential must have agreed to use barrier contraception for the duration of the study (Women of childbearing potential included all women except for those who are premenstrual, whose menstrual periods have not occured for greater than or equal to one year after menopause, who are surgically sterilized, or who have had a hysterectomy)
* Can understand and sign the informed consent document, can communicate with the investigator, and can understand and comply with the requirements of the protocol
Exclusion Criteria:
* Clinically relevant history or presence of respiratory, gastrointestinal, renal, hepatic, hematological, cardiovascular, psychiatric, musculoskeletal, genitourinary, immunological, dermatological, or connective tissue disease or disorder
* Clinically relevant surgical history
* History of alcoholism and/or drug abuse within the past 5 years
* Significant infection or known inflammatory process including viral infections
* Required prophylactic antibiotics for SBE (infectious endocarditis)
* Had acute gastrointestinal symptoms at screening and/or baseline
* Allergies to any of the following: lidocaine/epinephrine, articaine/epinephrine, prilocaine/epinephrine, bisulfites or metasulfites, or phentolamine
* Had used any investigational drug and/or participated in any clinical trial within 30 days of baseline
* Used pain relievers 24 hours prior to anesthetic administration
* Required the use of nitrous oxide or sedatives to perform the scheduled, eligible dental procedure
* Pregnancy, attempting to conceive,or lactating
* Used decongestants or other drugs with vasoactive moieties within 24 hours prior to anesthetic administration
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
10 Years
Maximum Age:
65 Years
Study:
NCT00154167
Study Brief:
Protocol Section:
NCT00154167