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Study on the diagnosis and treatment strategy of neurofibromatosis type 2 based on evidence-based medicine

Study on the diagnosis and treatment strategy of neurofibromatosis type 2 based on evidence-based medicine

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000036117
Enrollment
Unknown
Registered
2020-08-21
Start date
2020-10-01
Completion date
Unknown
Last updated
2020-08-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Neurofibromatosis type 2

Interventions

3:Cochlear implant
2:Treatment of Avastin
1:follow-up observation

Sponsors

Ninth Perople's Hospital, Shanghai Jiao Tong University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
3 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1. The clinically diagnosed patients with neurofibromatosis type 2 (NF2) and their family members who have obtained understanding through the education and education, all participants need to sign informed consent. 2. The age at diagnosis of NF2 is >= 3 years old.

Exclusion criteria

Exclusion criteria: (1) Inability to have full civil liability due to mental state; (2) According to clinical guidelines, neoadjuvant treatment must be performed before tumor tissue can be obtained by puncture or surgery; (3) Virus infection such as HIV, syphilis, gonorrhea; (4) Infections, mental disorders and other diseases in the ongoing or active period; (5) Currently participating in other drug intervention research clinical trials; (6) Are currently using anticoagulants (excluding contraceptives), have a history of bleeding or coagulation disorders; (7) Imaging shows hemorrhage within 6 months, or history of symptomatic intracranial hemorrhage, or any history of spontaneous intracranial hemorrhage; (8) Have autoimmune coagulopathy, including idiopathic thrombocytopenic purpura, etc.; (9) Those who cannot be followed up and evaluated as required; (10) Transplant recipient patients.

Design outcomes

Primary

MeasureTime frame
Size of tumor;Hearing evaluation;

Countries

China

Contacts

Public ContactWang Zhaoyan

Ninth Perople's Hospital, Shanghai Jiao Tong University School of Medicine

wzyent2019@163.com+86 13761000011

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026