Advantage of Tramadol in Local Analgesia Post-Sternotomy

Phase 4

Completed

• Conditions: Post-operative Analgesia; Heart Surgery Via Sternotomy
• Interventions: Drug: levobupivacaine; Drug: tramadol

• Registration Number: NCT02851394
• Lead Sponsor: Centre Hospitalier Universitaire Dijon

Brief Summary

Sternotomy, the reference approach for heart surgery, may induce profound and intense post-operative pain. One method of analgesia used is patient-controlled intravenous morphine.

The analgesic efficacy of continuous wound infiltration at the sternum following heart surgery has been demonstrated.

The analgesic catheter placed near the sternotomy wound reduces the consumption of morphine.

The aim of this study is to determine whether a bolus of tramadol associated with the continuous administration of levobupivacaine via the wound catheter could potentiate the local anaesthetic effects, thus leading to a decreased consumption of postoperative intravenous morphine, and a decrease in morphine-related side effects.

Detailed Description

Not available

Study Timeline

• Study Start: 2015-10
• Primary Completion: 2016-05
• Status Verified: 2016-07
• Study First Submitted: 2016-07-28
• Study First Submitted QC: 2016-07-29
• Study First Posted: 2016-08-01
• Study Completion: 2016-10
• Last Update Submitted: 2017-10-09
• Last Update Posted: 2017-10-10

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 160

Inclusion Criteria

• Persons who have provided written consent
• Patients over 18 years old
• Patients undergoing heart surgery via sternotomy: aortic valve surgery, mitral valve surgery, tricuspid valve surgery, atrial myxoma, coronary artery bypass graft, aorta surgery
• Patients undergoing emergency or scheduled surgery

Exclusion Criteria

• Adults under guardianship
• Persons without national health insurance cover
• Pregnant or breast-feeding women
• Patients already included in the study once
• Patients with aortic dissection
• Patients with mediastinitis or sternal nonunion
• Patients undergoing heart surgery for the second or more time
• Patients with local infection or generalized bacteraemia-type infection
• Patients with hypersensitivity to local anaesthetics or to tramadol or to opiates or to one of the excipients present in the products used
• Patients with hypersensitivity to paracetamol or to paracetamol hydrochloride (prodrug of paracetamol)
• Patients on antidepressants, gabapentin, pregabalin, neuroleptics
• Patients with a history of convulsions or epilepsy
• Patients with preoperative cognitive dysfunction
• Patients with intracranial hypertension
• Chronic use of morphines or high-dose steroid or non-steroid anti-inflammatory agents
• Patients with acute or chronic kidney failure (creatininemia > 170 µmol/L)
• Patients with liver failure or porphyria
• Patients under 17 years old
• Patients with severe respiratory failure
• Patients treated with a non-selective MAOI (iproniazid), a selective MAOI A (moclobemid, toloxatone), selective MAO-B inhibitor (Selegiline) or linezolid (Zyvoxid®)
• Patients with acute intoxication or an overdose of products that depress the central nervous system (alcohol, hypnotics, other analgesics...)
• Patients with severe hypotension

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Levobupivacaine group	levobupivacaine	-
Levobupivacaine + tramadol group	tramadol	-
Levobupivacaine + tramadol group	levobupivacaine	-

Primary Outcome Measures

Name	Time	Method
Consumption of morphine, expressed in milligrams, in the post-operative period	48 hour after extubation

Trial Locations

Locations (1)

CHU Dijon Bourgogne; 🇫🇷 Dijon, France