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 @ 3:56 AM
Ignite Modification Date:
2025-12-25 @ 3:56 AM
NCT ID:
NCT00657202
Eligibility Criteria:
Inclusion Criteria:
* Patients must have diagnosis of NF1 based on NIH criteria with two or more of the following characteristics: a) Six or more cafe-au-lait macules b) Skin fold freckling in the axilla or groin c) Optic pathway glioma d) Two or more Lisch nodules of the iris e) Distinctive bony lesions such as dysplasia of the sphenoid wing or of a long bone such as the tibia f) Two or more neurofibromas of any type or 1 or more plexiform neurofibroma g) First degree relative with NF1
* At least four cutaneous neurofibromas on skin exam with the following qualities: a) the lesion must be discrete by clinical exam and must be at least 5mm away from another skin tumor b) the lesion must be amenable to measurement with calipers with minimum dimension of 5mm and maximum dimension of 20mm c)the lesions cannot be located on the face, scalp, or groin and must be located in an area that can be photographed d) histologic confirmation of tumor type is not required in the setting of compatible clinical setting
* Must be willing to have treated CNF surgically removed during the study
* 18 years of age or older
* Normal organ and marrow function as described in the protocol
Exclusion Criteria:
* Pregnant or breast-feeding women
* Chemotherapy or radiotherapy within 6 weeks prior to entering the study
* Receiving any other investigational agent
* History of allergic reactions attributed to compounds of similar chemical or biologic composition as ranibizumab
* Hypertension that cannot be controlled by medications
* Known coagulopathy that increases risk of bleeding or a history of clinically significant hemorrhages in the past
* NCI CTCAE grade 3 hemorrhage within 4 weeks of starting the study treatment
* Pre-existing thyroid abnormality with thyroid function that cannot be maintained in the normal range with medication
* Uncontrolled intercurrent illness
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT00657202
Study Brief:
Protocol Section:
NCT00657202