Efficacy of Parasternal Blocks in Cardiovascular Surgery Patients Undergoing Median Sternotomy
Unknown statusNot applicableNCT06387095
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This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.
Brief summary (from the registry)
Acute and chronic pain after cardiac surgery is a common problem that negatively affects quality of life. Postoperative pain after cardiac surgery is most intense in the first two days and decreases in the following period. However, postoperative pain with incomplete management in the acute period may become chronic. This may negatively affect the patient's quality of life. Although central blocks such as thoracic epidural and paravertebral blocks are considered the gold standard in analgesia control, the advantages of thoracic plan blocks, which are more superficial due to peroperative heparinisation; coagulation disorders; and procedural difficulties, are undeniable. Thoracic plane blocks, which can also be used in patients receiving anticoagulant and/or antiplatelet therapy, have recently been used for acute pain. The aim of this study was to evaluate the effect of thoracic plane blocks on extubation time, pain scores, intensive care unit (ICU) and hospital stays in patients undergoing median sternotomy.
Study details
- Official title
- Efficacy of Parasternal Blocks in Cardiovascular Surgery Patients Undergoing Median Sternotomy: Randomized, Controlled Study
- Conditions
- Interventions
- Procedure: 1. no block
- Procedure: 2. superficial parasternal block
- Procedure: 3. deep parasternal block
- Sponsor
- Kartal Kosuyolu Yuksek Ihtisas Education and Research Hospital
- Start date
- 2024-02-01
- Primary completion
- 2024-04-16
- Sex
- All
- Age range
- from 18 Years to 80 Years
- Results posted
- No results posted in this snapshot
- Countries
- Turkey (Türkiye)
- Total sites listed
- 1
Eligibility criteria
Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * Performing median sternotomy * Elective case * Over 18 years of age; under 80 years of age * ASA II-III patients Exclusion Criteria: * Emergency cases * Patients undergoing minimally invasive surgery * Patients with a history of opioid use in the last 30 days * Redo cases * Patients with left ventricular ejection fraction less than 30% * Patients with severe hepatic or renal insufficiency * Patients with chronic pain before surgery (migraine, fibromyalgia)
Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT06387095