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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03719781
Other study ID # GOKAEK 2017/153
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date November 2018
Est. completion date March 2019

Study information

Verified date October 2018
Source Kocaeli University
Contact Cennet Tor Kiliç
Phone +903038248
Email cennetmfk34@gmail.com
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

As postoperative cognitive dysfunction rates are high especially in elder patients, cognitive dysfunction is not diagnosed and treated effectively. This statement is associated with prolonged hospital stays by increasing morbidity. We wanted to see the incidency of postoperative cognitive dysfunction in patients undergoing elective pituitary tumor removal surgery.


Recruitment information / eligibility

Status Recruiting
Enrollment 90
Est. completion date March 2019
Est. primary completion date February 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria:

- ASA I-II patients

- Undergoing elective pituitery tumor removal surgery

Exclusion Criteria:

- >II ASA scores

- Using antidepressant agents

- Patient refusal

- Mental diseases

Study Design


Intervention

Diagnostic Test:
standardized minimental testing
To diagnose postoperative cognitive dysfunction

Locations

Country Name City State
Turkey Kocaeli University Kocaeli

Sponsors (1)

Lead Sponsor Collaborator
Kocaeli University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary minimental test score scores between 0-30 preoperative 24th hour
Primary minimental test score scores between 0-30 postoperative 4th hour
Primary minimental test score scores between 0-30 postoperative 24th hour
Primary minimental test score scores between 0-30 one month after discharged
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