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COMPLETED
NCT03090776
EARLY_PHASE1

Prevention of Post Mastectomy With Intraoperative Ketamine

Sponsor: Brigham and Women's Hospital

View on ClinicalTrials.gov

Summary

Aim 1: To determine the effectiveness of perioperatively administered ketamine to decrease acute and persistent postmastectomy pain (PPMP). Hypothesis 1.1: Patients undergoing partial or total mastectomy treated with a bolus and perioperative infusion of the NMDA-receptor antagonist ketamine will have decreased postoperative pain and opioid utilization compared to those receiving saline control. Hypothesis 1.2: Patients undergoing partial or total mastectomy treated with a bolus and perioperative infusion of the NMDA-receptor antagonist ketamine will have decreased persistent postoperative pain measured at one year after surgery. Aim 2: To determine whether there is increased power to detect therapeutic effectiveness in an interventional preventive trial, by enrichment with patients at high risk of PPMP. Hypothesis 2.1: Ketamine will have a greater analgesic and opioid sparing effect on pain scores in high-risk patients than non-high risk patients, compared to placebo. Hypothesis 2.2: Ketamine will have a greater preventive effect on pain burden scores at one year after surgery in high-risk patients than non-high risk patients, compared to placebo.

Official title: Prevention of Post-Mastectomy Pain With Perioperative Ketamine Administration: A Randomized, Placebo-controlled Trial

Key Details

Gender

FEMALE

Age Range

18 Years - 85 Years

Study Type

INTERVENTIONAL

Enrollment

264

Start Date

2017-07-01

Completion Date

2025-09-01

Last Updated

2026-07-20

Healthy Volunteers

No

Interventions

DRUG

Ketamine

low dose bolus and infusion ketamine, administered under general anesthesia

OTHER

Placebo saline

bolus and infusion saline, administered under general anesthesia

Locations (1)

Brigham and Women's Hospital

Boston, Massachusetts, United States