The Effect of Paravertebral Block on Recovery After CABG Surgery

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorAdiyaman University Research Hospital

About this trial

The study aims to evaluate the analgesic efficacy of paravertebral block, mobilization speed, respiratory functions, and complication rates in patients who have undergone cardiac surgery and are monitored in the intensive care unit during the postoperative period.

Eligibility criteria

Qualifiers

Patients aged 18 and older scheduled for elective coronary artery bypass graft surgery with median sternotomy

Disqualifiers

Contraindications to neuroaxial block ( coagulopathy, infection at the injection site, allergy to local anesthetics..)

Emergency surgeries

severe back deformities

Chronic pain

Trial design

Treatments tested in this trial

  • paravertebral block

Treatment groups

120 Participants
are divided into 2 treatment groups

Locations

This trial has no locations