RECRUITING

Magnesium Sulfate as an Adjunctive Analgesic in Prostate Surgery

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The purpose of this clinical trial is to determine if receiving magnesium sulfate as an adjunctive analgesic for prostate surgery is effective in reducing pain. Subjects will be randomized to receive magnesium or not receive it, as part of a standardized general anesthetic for prostate surgery. The primary objective is to demonstrate improved pain scores in patients receiving magnesium sulfate as an adjunctive analgesic during surgery. Secondary objectives include demonstrating reduced requirements for other opioids, reduced postoperative shivering, improved discharge home and adequate neuromuscular blockade reversal, measured by quantitative train of four monitoring.

Official Title

A Randomized, Controlled Trial of Magnesium Sulfate as an Adjunctive Analgesic in Prostate Surgery

Quick Facts

Study Start:2024-06-04
Study Completion:2025-06
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06477133

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:MALE
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. 1. Age 18 and older.
  2. 2. Undergoing a robotic prostatectomy under general anesthesia.
  3. 3. Is willing and able to provide consent to participate in the study.
  1. 1. Patients younger than 18 years
  2. 2. Patients with end-stage renal disease
  3. 3. Known allergy to magnesium sulfate preparations
  4. 4. Any patient that the investigators feel cannot comply with all study related procedures

Contacts and Locations

Study Contact

Mark Nunnally, MD
CONTACT
212-263-2087
nunnally@nyulangone.org

Principal Investigator

Mark E. Nunnally, MD
PRINCIPAL_INVESTIGATOR
NYU Langone Health

Study Locations (Sites)

NYU Langone Health
New York, New York, 10016
United States

Collaborators and Investigators

Sponsor: NYU Langone Health

  • Mark E. Nunnally, MD, PRINCIPAL_INVESTIGATOR, NYU Langone Health

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-06-04
Study Completion Date2025-06

Study Record Updates

Study Start Date2024-06-04
Study Completion Date2025-06

Terms related to this study

Keywords Provided by Researchers

  • Prostate surgery
  • analgesia

Additional Relevant MeSH Terms

  • Prostatectomy