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NCT03865550

Post-op Ketamine Study

Status unknown NA Last updated 7 March 2019
What this trial tests

NA trial testing Isotonic saline in Osteo Arthritis Knee in 75 participants. Status unknown.

Timeline
28 March 2016
Primary endpoint
27 April 2018
27 April 2019

Quick facts

Lead sponsorRothman Institute Orthopaedics
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingquadruple
Primary purposetreatment
Enrollment75
Start date28 March 2016
Primary completion27 April 2018
Estimated completion27 April 2019
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Rothman Institute Orthopaedics

Who can join

Eligibility, any sex, with Osteo Arthritis Knee. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this study is to establish the effect of sub-anesthetic dosing of ketamine with spinal anesthesia during total knee arthroplasty on post-operative pain and narcotic consumption. We hypothesize that sub-anesthetic ketamine will decrease post-operative pain and narcotic consumption and may secondarily lead to shorter lengths of stay, faster rehabilitation, improved postoperative outcomes and patient satisfaction.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Isotonic saline

Trials testing the same drug.

Other recruiting trials for Osteo Arthritis Knee

Currently open trials in the same condition.

Other Rothman Institute Orthopaedics trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03865550.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing