Medical Services

Clinical Trials at Englewood Hospital: Anesthesiology

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EHMC IRB Study #: E-13-512

Principal Investigator:
Dr. Aryeh Shander
Tel: 201-894-3238
Email: aryeh.shander@ehmc.com

Study Coordinator:
Sajjad Naqvi
Tel: 201-894-3917
Email: sajjadnaqvi25@gmail.com

Sponsor:
Masimo Corporation

Study Title:
Prospective observational study characterizing noninvasive hemoglobin (SpHb) measured with Pulse CO-Oximetry technology, in a variety of surgical cases

Eligibility requirements:
Patients who are at least 18 years old and are scheduled for a surgery under general anesthesia.

Study objectives:
The purpose of the study is to collect data to characterize Masimo's non-invasive Rainbow technology during surgeries on patients. The results of the non-invasive measurement will be compared to that obtained from the standard analysis of blood samples routinely collected during surgery to monitor hemoglobin levels.

Procedures:
Subjects who consent to participate will have up to 6 external monitors placed on their fingers, forehead, neck, chest, or ears. In addition to the standard blood drawn during surgery for monitoring of hemoglobin, a maximum of five additional blood draws may be performed for study purposes.

*This is only a summary of the study information. Please contact the Principal Investigator or Study Coordinator for the full details.

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EHMC IRB Study #: E-07-313 

Principal Investigator:
Dr. Aryeh Shander
Tel: 201-894-3238
Email: aryeh.shander@ehmc.com

Study Coordinator:
Sajjad Naqvi
Tel: 201-894-3917
Email: sajjadnaqvi25@gmail.com

Sponsor:
Mount Sinai School of Medicine

Study Title:
Dexlirium Trial: Perioperative Cognitive Protection - Dexmedetomidine and Cognitive Reserve

Eligibility requirements:
Patients who are at least 68 years old, and who are scheduled for major surgery to be performed under general anesthesia.

Study objectives:
To test the influence of Dexmedetomidine ("Dex") as compared to placebo on post-surgery delirium and cognitive function in elderly patients.

Procedures:
Subjects will be randomized to receive either Dex (an FDA-approved sedative) or placebo in addition to the routine anesthesia given during surgery. Study personnel will administer interviews and memory tests before, and at several time points after, surgery to assess cognitive function.

*This is only a summary of the study information. Please contact the Principal Investigator or Study Coordinator for the full details.

 

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