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 @ 12:54 AM
Ignite Modification Date:
2025-12-25 @ 12:54 AM
NCT ID:
NCT00762567
Eligibility Criteria:
Inclusion Criteria:
* Male and female children and adolescents, ages 2 to \< 18 years, with a minimum weight of 24 pounds will be eligible to participate. In addition, each subject will be \> 5th percentile and \< 95th percentile for weight based on age and gender.
* Subjects will have a body mass index (BMI) \> 5th percentile and less than or equal to the 90th percentile for age and gender.
* Subjects who have a history of allergic rhinitis and who are experiencing nasal symptoms associated with hay fever or other upper respiratory allergies will be included.
* Subjects and parents or legally authorized representatives who, in the investigator's view, are likely to be compliant and complete the study will be eligible to participate.
* Post menarchal female subjects must have a negative urine pregnancy test at screening and at Visit 2 on Day 1 before study medication is administered.
* Post menarchal female subjects must have practiced abstinence or use an effective form of birth control (e.g., intrauterine device, oral contraceptives, contraceptive implants or injections, diaphragm with spermicide, cervical cap, or consort use of condom) for at least three months before being enrolled in the study.
* Parents or legally authorized representatives have signed and dated an IRB-approved consent form for the subject to participate in the study indicating that the subject (and/or a legally acceptable representative) has been informed of all pertinent aspects of the study.
* Subjects, ages 6 to \< 18 years, who have provided written assent to participate in the study
Exclusion Criteria:
* Evidence or history of clinically significant hematological, renal, endocrine, pulmonary, gastrointestinal, cardiovascular, hepatic, psychiatric, or neurologic disease.
* Findings from the medical history or physical examination with vital sign measurements that are not within the range of clinical acceptability.
* Have a known sensitivity or allergy to phenylephrine or EMLA cream.
* Took any prescription or nonprescription medication (except vitamins and/or fluoride supplements) within seven days before the study's start date.
* Drank any fruit juices (i.e., apple, orange, or grapefruit) within two days prior to the study start.
* Use of any monoamine oxidase inhibitor within two weeks prior to the dose of phenylephrine.
* Participated in, or completed, another clinical trial within seven weeks before the study's start date.
* Have a history of drug, alcohol, and tobacco use (older children and adolescents).
* Have a history of hepatitis B, a previous positive test for hepatitis B surface antigen, or a previous positive hepatitis C antibody.
* Have a history of HIV infection or previous demonstration of HIV antibodies.
* Pregnant or nursing females; females of childbearing potential who are unwilling or unable to use an acceptable method of nonhormonal contraception from at least three months prior to the first dose of study medication until completion of follow-up procedures.
* Relationship to persons involved directly with the conduct of the study (ie, principal investigator; subinvestigators; study coordinators; other study personnel; employees or contractors of the sponsor or its subsidiaries; and the families of each).
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
2 Years
Maximum Age:
17 Years
Study:
NCT00762567
Study Brief:
Protocol Section:
NCT00762567