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Neurofibromatosis 2 clinical trials

View clinical trials related to Neurofibromatosis 2.

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NCT ID: NCT03617276 Completed - Neurofibromatosis 2 Clinical Trials

Reliability of Functional Outcome Measures in Neurofibromatosis 2

Start date: September 7, 2016
Phase:
Study type: Observational

Neurofibromatosis 2 (NF2) is a rare inherited condition. Those with NF2 usually present with tumours (schwannomas) in their inner ear, or vestibular organ, with common symptoms including problems with hearing, balance, dizziness and vision. This study aims to evaluate the reliability (stability) of a range of functional standardised outcome measures in adults with NF2.

NCT ID: NCT03210285 Completed - Clinical trials for Vestibular Schwannoma

WES of NF2-associated in Comparison to Sporadic Vestibular Schwannomas - Correlation With Clinical Data

NF2
Start date: July 31, 2017
Phase:
Study type: Observational [Patient Registry]

Whole exome sequencing (WES) of 50 sporadic and 50 Neurofibromatosis Type2 (NF2)-associated vestibularis schwannomas (VS) in children and young adults. The aim is to gain insight into the complete genome of the NF2 associated VS compared to sporadic VS (control group). These data are to be correlated with the clinic, ie the auditory function (audiogram, acoustically evoked potentials) and the clinical picture as well as the tumor growth rate and general data such as sex, age, side, etc.

NCT ID: NCT02934256 Completed - Clinical trials for Vestibular Schwannoma

Icotinib Study for Patients With Neurofibromatosis Type 2 (NF2) and NF2-Related Tumors

Icotinib
Start date: July 2016
Phase: Phase 2
Study type: Interventional

1)Preliminarily evaluate the treatment effect of Icotinib Hydrochloride Tablets on NF2; 2)Preliminarily evaluate the safety and the patient's tolerance of the treatment of Icotinib; 3)Provide an objective basis for an enlarged randomized double-blind trial.

NCT ID: NCT02831257 Completed - Meningioma Clinical Trials

AZD2014 In NF2 Patients With Progressive or Symptomatic Meningiomas

Start date: August 31, 2016
Phase: Phase 2
Study type: Interventional

The goal of this clinical research study is to learn if the study drug AZD2014 can shrink growing or symptomatic meningiomas.

NCT ID: NCT02811718 Completed - Neurofibromatosis 2 Clinical Trials

Resiliency Training for Patients With NF2 Via Videoconferencing With Skype

Start date: July 2016
Phase: N/A
Study type: Interventional

The aim of this study is to determine, whether the 3RP is feasible, accepted and efficacious and durable when delivered via Skype to patients with neurofibromatosis type 2 (NF2) who are deaf or have severe hearing loss using Communication Access Realtime Translation (CART) and/or American Sign Language (ASL). This will be a substudy of the IRB-approved protocol #2013P002605. It is the same study except it is looking at a particular sub-population: patients with NF2 who are hard of hearing.

NCT ID: NCT02298270 Completed - Neurofibromatosis 2 Clinical Trials

Resiliency Training for Patients With Neurofibromatosis Via Videoconferencing With Skype

Start date: March 2014
Phase: N/A
Study type: Interventional

This study tests the efficacy of an 8-week, Skype-based, group resiliency training intervention (The Relaxation Response Resiliency Program) for improving psychological stress in patients with Neurofibromatosis. A control group will receive a general health education curriculum. The investigators hypothesize that patients will improve on measures of psychological stress as a result of the resiliency program. A substudy (Unique Protocol ID: 2013P002605b) has been approved to test this study on a sub-population: patients with NF2 who are hard of hearing.

NCT ID: NCT02246231 Completed - Clinical trials for Neurofibromatosis Type 2

Effect of Implant Position on Magnetic Resonance Image Distortion

Start date: February 3, 2014
Phase: N/A
Study type: Interventional

Patients with Neurofibromatosis type 2 (NF2) almost always develop acoustic neuromas in both ears. As a result of the tumours themselves or the treatment of the tumours, many patients become profoundly deaf in both ears. It is possible to restore a degree of hearing by placing a hearing implant in the brainstem adjacent to the hearing pathways within the brain. This is termed an auditory brainstem implant (ABI). The aim of this study is to find the optimum head position in relation to the MRI magnet field, which would produce least area of image distortion in patients with ABIs. This will be of benefit in optimising the MR imaging in future patients with implants.

NCT ID: NCT02129647 Completed - Clinical trials for Neurofibromatosis Type 2

Study of Axitinib in Patients With Neurofibromatosis Type 2 and Progressive Vestibular Schwannomas

Start date: April 2014
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine if the study drug, AXITINIB, has any effect on tumors found in patients with Neurofibromatosis Type 2 (NF2).

NCT ID: NCT02104323 Completed - Clinical trials for Vestibular Schwannoma

Endostatin Study for Patients With Neurofibromatosis Type 2 (NF2) and NF2-Related Tumors

Endostatin
Start date: January 2014
Phase: Phase 2
Study type: Interventional

1)Preliminarily evaluate the treatment effect of continuous vein injection of recombinant human endostatin on NF2; 2)Preliminarily evaluate the safety and the patient's tolerance of the treatment of endostatin; 3)Provide an objective basis for an enlarged randomized double-blind trial.

NCT ID: NCT01880749 Completed - Clinical trials for Neurofibromatosis Type 2

Exploring the Activity of RAD001 in Vestibular Schwannomas and Meningiomas

Start date: June 2013
Phase: Early Phase 1
Study type: Interventional

The primary objective is to estimate the proportions of vestibular schwannomas (VS) and meningiomas after 10 days of exposure to the study drug RAD001 at a dose of 10 mg daily, as determined by immunohistochemistry. This is a "phase 0" PK (pharmacokinetic) and PD (pharmacodynamic) study of RAD001 in patients with Neurofibromatosis Type 2-related and sporadic VS and meningiomas. Enrolled patients will take RAD001 prior to a scheduled VS or meningioma surgery, and blood and tissue samples will be obtained for further analysis.