Safety Study of Hemospan® in Prostatectomy Patients

Completed · Phase 2

Conditions studied: Blood Loss, Surgical, Prostate Cancer, Surgery

In brief

This is a progressive dose escalation study designed to evaluate the safety of Hemospan compared to a standard crystalloid solution (Ringer's lactate) in elective surgery patients undergoing total prostatectomy procedures with anticipated blood loss of more than 500 mL. Secondary objectives of this study are to observe possible activity of Hemospan for tissue oxygenation, perfusion and cardiovascular support.

Key facts

Study ID

NCT00425334

Run by

Sangart

People needed

20

Starts

2005-07-01

Expected to finish

2007-11-01

Last updated by the study team

2013-08-19

Who can join

Age: 18 and older. Sex: male. Healthy volunteers: not accepted.

You may qualify if…

• Adult male ASA class I or II patients over the age of 18 scheduled for elective total prostatectomy surgery with anticipated blood loss greater than 500 mL
• Patients must be in good health (other than the indication for prostatectomy surgery) as determined by medical history, physical examination, clinical laboratory studies and electrocardiogram (ECG)
• At screening (within 2 weeks of the scheduled surgery) the blood chemistry and hematology (Hb, Hct, RBC, WBC, platelets, PT, PTT, plasma fibrinogen, fibrin split products and haptoglobin) must be within the laboratory normal limits
• Patients must test negative for HIV and hepatitis screens
• Patients must sign an Informed Consent Form (see Appendix II) for the study, which has been reviewed and approved by the Institutional Review Board, prior to screening and entry into the study
• Patients must be available within the continental United States for the period of this study, and willing to complete the follow-up at 4-6 weeks
• Patients must be able to understand and read English

You may not qualify if…

• Any acute or chronic condition which would limit the patient's ability to complete the study or jeopardize the safety of the patient
• History or clinical manifestations of a significant cardiovascular or pulmonary disorder
• Clinically significant psychiatric disorder requiring active treatment
• History of diabetes requiring active treatment
• History or clinical manifestation of significant renal or hepatic disorder
• History of thyroid disease or clinical symptoms consistent with thyroid disease
• History of bleeding disorder
• History or family history of a hemoglobinopathy
• Patients with contraindications to TEE probe insertion
• Patients who have received any other investigational drugs within 30 days prior to administration of the study drug
• Professional or ancillary personnel involved with this study

Where it is running

• Johns Hopkins Medical Institutions — Baltimore, Maryland, United States

Full record on ClinicalTrials.gov

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