Clinical Trials Directory

Trials / Completed

CompletedNCT04129086

Ketamine for Acute Pain Management After Trauma

Ketamine for Acute Pain After Trauma: KAPT Trial

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
305 (actual)
Sponsor
The University of Texas Health Science Center, Houston · Academic / Other
Sex
All
Age
16 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to compare the effectiveness of Ketamine drip along with usual care and usual care alone on trauma patients and to longitudinally quantify the pain experience of patients during hospitalization.

Conditions

Interventions

TypeNameDescription
DRUGKetamine plus usual careBolus of .35 mg/kg Infusion start @ 0.15 mg/kg/hr; titrate range is 0.1 - 0.25 mg/kg/hr for 24 to 48 hours after admission and each subsequent major surgery plus multi-modal pain therapy considered as standard of care. Standard of care medications include Acetaminophen 1000 mg po q6 hours, Naproxen 500 mg po q12 hours, Gabapentin 300 mg po q8 hours and Lidocaine patch q 12 hours.
DRUGUsual CareStandard of care medications include Acetaminophen 1000 mg po q6 hours, Naproxen 500 mg po q12 hours, Gabapentin 300 mg po q8 hours and Lidocaine patch q 12 hours.

Timeline

Start date
2020-07-01
Primary completion
2022-03-30
Completion
2022-09-30
First posted
2019-10-16
Last updated
2023-04-21
Results posted
2023-04-21

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT04129086. Inclusion in this directory is not an endorsement.