Clinical Trials Logo

Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01377701
Other study ID # KY2010-259
Secondary ID
Status Recruiting
Phase N/A
First received June 20, 2011
Last updated June 20, 2011
Start date June 2011
Est. completion date December 2012

Study information

Verified date June 2011
Source Huashan Hospital
Contact Yao Zhao, M.D.
Phone 86-13916872553
Email zhaoyaohs@vip.sina.com
Is FDA regulated No
Health authority China: Food and Drug Administration
Study type Observational

Clinical Trial Summary

Pituitary adenomas can cause compression of optic nerves and chiasm, which will lead to damage of vision. This study aims to evaluate the predictive factors for recovery of vision in patients with pituitary adenomas following trans-sphenoidal surgery.


Recruitment information / eligibility

Status Recruiting
Enrollment 150
Est. completion date December 2012
Est. primary completion date December 2012
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

- >18 years old

- patients with pituitary adenomas, loss of visual field

- patients receive trans-sphenoidal surgery

Exclusion Criteria:

- visual damage caused by other diseases

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Locations

Country Name City State
China Huashan Hospital Shanghai

Sponsors (1)

Lead Sponsor Collaborator
Huashan Hospital

Country where clinical trial is conducted

China, 

See also
  Status Clinical Trial Phase
Recruiting NCT01442220 - Genome-wide Association Study of Pituitary Tumors N/A
Completed NCT02803697 - Predictive Factors of Recurrence of Non Functioning Pituitary Adenomas : a Retrospective Study of 220 Patients in the Reims University Hospital, France
Completed NCT00939523 - Targeted Therapy With Lapatinib in Patients With Recurrent Pituitary Tumors Resistant to Standard Therapy Phase 2
Not yet recruiting NCT04244708 - The Effect of Chemoradiotherapy in Patients With Refractory Pituitary Adenomas Phase 2/Phase 3