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Finding best practice: use of s-ketamine peropertively and in patient controlled analgesia in the treatment of pain after major abdominal surgery

Recruiting
Conditions
Analgesia in abdominal surgery
10062915
10043413
Registration Number
NL-OMON32227
Lead Sponsor
Erasmus MC, Universitair Medisch Centrum Rotterdam
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Not specified
Target Recruitment
50
Inclusion Criteria

The patient has provided written informed consent prior to admission to the study
The patient is between 18 and 70 years of age

Exclusion Criteria

The patient has a history of uncontrolled chronic disease which would contra-indicate study participation.
The patient has severe systemic disease that limits activity and is a constant threat to life (ASA IV).
The patient has a history of chronic substance abuse within the last 3 months.
The patient has a history of psychiatric disorders.
The patient has a history of hypersensitivity to one of the study drugs.
The patient has a history of severe chronic respiratory disorders.
The patient is either breastfeeding or pregnant.

Study & Design

Study Type
Observational invasive
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<p>1. The total morphine use over 72 hours.<br /><br>2. The occurence of side effects.<br /><br>3. The VAS scores per study group.</p><br>
Secondary Outcome Measures
NameTimeMethod
<p>1. Evaluation of the levels of the amino-acids (glutamate, glycine, tryptofane,<br /><br>arginine e.g) and the effect of analgesia on them.</p><br>
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