Prostate Cancer Clinical Trial

The Effect of Deep Versus Moderate Muscle Relaxants in Men During and After Robotic Surgery for Prostate Cancer

Summary

The purpose of this study is to determine if there is a difference in intra-abdominal pressure which surgeons use during surgery and post-surgery pain in men who undergo robotic prostate surgery with deep neuromuscular blockade (NMB), compared with moderate NMB.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Adult patients under the age of 80
American Society of Anesthesiologists Physical Status 1, 2, 3.
Elective Robotic Prostatectomy
Patient undergoing surgery at Josie Robertson Surgical Center

Exclusion Criteria:

Age younger than 18
Inability to provide informed consent
Allergy to rocuronium, sugammadex, midazolam, propofol, fentanyl, lidocaine, mannitol (IV Acetaeminophen), IV Acetaminophen, Ketorolac, Morphine, Hydromorphone, Dexamethasone, Zofran, Benadryl, Compazine
Neuromuscular disease
Any patient with previous abdominal surgery less than or equal to 20 years prior to scheduled surgery date
Patients with BMI>35
Severe renal impairment (Creatinine clearance < 30 ml/min)
Patient receiving Toremifene or any history of receiving Toremifene
Chronic pain patients
Patients receiving suboxone
Patients receiving succinylcholine

Study is for people with:

Prostate Cancer

Phase:

Phase 2

Estimated Enrollment:

130

Study ID:

NCT03808077

Recruitment Status:

Recruiting

Sponsor:

Memorial Sloan Kettering Cancer Center

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There is 1 Location for this study

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Memorial Sloan Kettering Cancer Center
New York New York, 10065, United States More Info
Elizabeth Rieth, MD
Contact
212-639-5737

How clear is this clinincal trial information?

Study is for people with:

Prostate Cancer

Phase:

Phase 2

Estimated Enrollment:

130

Study ID:

NCT03808077

Recruitment Status:

Recruiting

Sponsor:


Memorial Sloan Kettering Cancer Center

How clear is this clinincal trial information?

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