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NCT03808077Active, not recruitingPhase 2

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

A Randomized Controlled Trial to Compare the Effectiveness of Deep vs. Moderate Neuromuscular Blockade in Reducing Postoperative Pain and Intra-Abdominal Insufflation Pressure During Minimally Invasive Robotic Prostatectomy

Source: ClinicalTrials.gov · Last updated 9 Mar 2026

Brief summary (registry, in English)

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.

Status (registry)
Active, not recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
139 (actual)
First submitted
15 Jan 2019
Start date
14 Jan 2019
Primary completion date
11 Oct 2024
Lead sponsor
Memorial Sloan Kettering Cancer Center
NCT number
NCT03808077

What you commit to

  • Study type: Interventional · Phase 2
  • Participants enrolled: 139
  • From 14 Jan 2019 to the primary completion date, 11 Oct 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Any patient with previous abdominal surgery less than or equal to 20 years prior to scheduled surgery date
  • Patient receiving Toremifene or any history of receiving Toremifene
  • Patients receiving suboxone
  • Patients receiving succinylcholine

Other illness

  • Allergy to rocuronium, sugammadex, midazolam, propofol, fentanyl, lidocaine, mannitol (IV Acetaeminophen), IV Acetaminophen, Ketorolac, Morphine, Hydromorphone, Dexamethasone, Zofran, Benadryl, Compazine
  • Neuromuscular disease

Lab values

  • Severe renal impairment (Creatinine clearance \< 30 ml/min)

Age

  • Age younger than 18

Other

  • Inability to provide informed consent
  • Patients with BMI\>35
  • Chronic pain patients

Who the study is looking for

  • 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

Age in the registry: 18 years to 80 years · Sex: Male · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Memorial Sloan-Kettering Cancer Center
Coordinator of this site? Confirm its status
New YorkUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.