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Postoperative Delirium in Patients Undergoing Radical Cystectomy

NCT03132168 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2021-08-27

No results posted yet for this study

Summary

In this study, post-operative delirium will be measured in patients undergoing surgery for bladder resection, and associated microRNA biomarkers will be evaluated in patients considered delirious and non-delirious after surgery.

Conditions

  • Post-operative Delirium

Interventions

BEHAVIORAL

Assessments

These cognitive assessments will be utilized during the study to evaluate cognitive levels comparing prior to surgery and post-operatively in order to determine if the subject is delirious. BIS monitoring will be utilized for all subjects.

PROCEDURE

Blood Draw

Subjects will have blood draws at surgical preadmission visit, Day 1, Day 2, and Day 3 post surgery only; one tube containing approximately one teaspoon (5 mL) of blood will be drawn at each visit.

OTHER

Standardized Anesthetic Care

Standardized anesthetic care will be provided as described by the protocol for each subject consented for this trial.

Sponsors & Collaborators

  • Ohio State University

    lead OTHER

Principal Investigators

  • Ahmad Shabsigh, MD · Ohio State University

Study Design

Allocation
NA
Purpose
OTHER
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-01-10
Primary Completion
2021-01-31
Completion
2021-01-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03132168 on ClinicalTrials.gov