Clinical trial

Efficiency and Safety a Fixed Combination of Orphenadrine and Diclofenac for Postoperative Analgesia in Cardiac Surgery Patients

Name
00191200
Description
The study will include 60 patients after cardiac surgery. The first group will include 30 patients who will use the drug Neodolpasse manufactured by Fresenius Kabi, which is a fixed combination of 30 mg of orphenadrine and 75 mg of diclofenac; the second group will consist of 30 patients who will use patient-controlled morphine analgesia (РСА) in the form of monotherapy.
Trial arms
Trial start
2022-03-18
Estimated PCD
2022-08-20
Trial end
2022-08-20
Status
Completed
Treatment
Analgesics Non Opioid (Neodolpasse manufactured by Fresenius Kabi)
A decrease in the pain severity (VAS);opioid-sparing effect
Arms:
the first group: a fixed combination of Orphenadrine and Diclofenac
Other names:
Fixed combination of Orfenadrine and Diclofenac
Analgesics
A decrease in the pain severity (VAS)
Arms:
the second group: patient-controlled analgesia (РСА) with Morphine
Other names:
Patient-controlled analgesia (with Morphine)
Size
60
Primary endpoint
visual-analog scale
hospitalisation period, an average of 24 hours
Eligibility criteria
Inclusion Criteria: 1. age from 18 years to 80 years inclusive 2. surgical access - median sternotomy 3. the first 2 hours after tracheal extubation 4. clear consciousness and productive contact with the patient 5. absence of erosive or ulcerative lesions of the mucous membrane of the esophagus, stomach and duodenum during preoperative esophago-gastro-duodenoscopy and clinical manifestations of gastrointestinal bleeding 6. no signs of renal dysfunction (KDIGO 0) 7. stable state of hemodynamics Exclusion Criteria: 1. a history of mental illness 2. the presence of contraindications to the appointment of diclofenac and orphenadrine or individual intolerance to drugs of these groups 3. renal and hepatic insufficiency 4. perioperative brain lesions 5. postoperative bleeding\>1.4 ml/kg/hour 6. severe cardiovascular (inotropic index\>10) and/or respiratory (RaO2 /FiO2\<200 mmHg) insufficiency
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['NA'], 'designInfo': {'allocation': 'RANDOMIZED', 'interventionModel': 'PARALLEL', 'primaryPurpose': 'TREATMENT', 'maskingInfo': {'masking': 'NONE'}}, 'enrollmentInfo': {'count': 60, 'type': 'ACTUAL'}}
Updated at
2023-08-22

1 organization

2 products

1 indication

Indication
Analgesic
Product
Analgesics