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MEDIPOL HOSPITAL 36

Recto-intercostal fascial plane block and pecto-intercostal fascial plane block for cardiac surgery
Source : Importé depuis le centre

Référence clinicaltrials.gov: NCT06285773
Cardiac surgery
Postoperative analgesia management
Recto-intercostal fascial plane block
Pecto-intercostal fascial plane block
Source :Importé depuis le centre
Recrutement fermé
Dernière modification : 2026/02/12
Type de recherche

Interventionnel


Population cible

Condition médicale (spécialité visée)

Donnée non disponible

Profil des participants

Limites d'âge
minimum : 18 ans maximum : 75 ans
Sexe(s) des participants

ALL

Source : Importé depuis le centre

Critères de sélection

Critères d'inclusion

Inclusion Criteria:

* American Society of Anesthesiologists (ASA) classification I-III
* Scheduled for cardiac surgery with elective median sternotomy under general anesthesia

Exclusion Criteria:

* a personal or family history of malignant hyperthermia,
* opioid sensitivity,
* alcohol or drug addiction,
* liver or kidney disease,
* skin infection in the area to be blocked,
* thoracic deformity,
* patients who are allergic to their medications,
* patients who do not agree to participate

Source : Importé depuis le centre

Thérapie ou Intervention proposée

Cohortes
Nom Condition médicale Traitement État du recrutement
Group PR = RIFPB and PIFB group Recto-intercostal fascial plane block (RIFPB) and Pecto-intercostal fascial plane block (PIFB) will be applied Donnée non disponible
  • Inconnu
  • Group Control No block will be applied. Donnée non disponible
  • Inconnu
  • Group PR = RIFPB and PIFB group
    État du recrutement
    unknown
    Group Control
    État du recrutement
    unknown
    Données à jour depuis : 12 février 2026

    Description de l'étude

    Résumé de l'étude

    In cardiac surgeries performed with median sternotomy, mediastinal and thoracic tube placement sites are outside the area of effect of parasternal blocks, and sometimes the sternotomy incision extends below the T6 dermatome. Recto intercostal fascial plane block (RIFPB) has been defined as a complementary block for analgesia of this region. This study aims to evaluate the effectiveness of the combination of ultrasound-guided recto-intercostal fascial plane block and pectointercostal fascial block for postoperative analgesia management after open heart surgery (coronary artery bypass) with median sternotomy.

    Source : Importé depuis le centre

    Open heart surgery is defined as surgery performed on the heart valves, arteries, and other heart structures by cutting the sternum with a median sternotomy. Cardiovascular diseases are prevalent in the general global population and affect most of the older adult population. With the increase in life expectancy in recent years, there has been a significant increase in surgical procedures for cardiovascular diseases. ERAS recommends effective perioperative pain control to improve outcomes after Cardiac Surgery. Inadequate pain control after open heart surgery causes decreased mobilization, increased respiratory complications, prolonged hospital stays, and chronic pain.

    Post-heart surgery pain is most intense during the first two days and then decreases. Considering that 17% of patients report chronic pain after cardiac surgery, it is crucial to provide effective analgesia in the early postoperative period.

    Failure to adequately relieve post-operative pain may lead to increased pulmonary complications as a result of inability to breathe deeply, coughing due to fear of pain, and consequent inability to clear bronchial secretions. Moreover, increased endogenous catecholamines due to surgery and pain increase the heart's oxygen consumption by causing tachycardia and hypertension. This situation causes ischemia, heart failure, and arrhythmias in patients who have undergone cardiac surgery.

    In general, postoperative pain is reduced with opioids, which can cause various complications. Although the use of opioids is recommended in cardiac surgery due to their ischemic effects, multimodal perioperative pain management strategies are recommended in current anesthesia. The use of regional anesthesia as part of multimodal strategies is steadily increasing in cardiac surgeries performed through median sternotomy. Despite multimodal analgesia strategies using regional techniques, post-operative pain still emerges as an important problem in open heart surgery with median sternotomy.

    The leading causes of pain after cardiac surgery are; sternotomy incisions, chest retraction, dissection of the internal mammary artery, thoracic tubes, sternal wires, and visceral pain. Sternal pain is transmitted through intercostal nerves originating from T2-T6 spinal nerve roots, whereas various regional techniques are used for analgesia in parasternal region surgeries. Amongst these techniques, while parasternal blocks can be preferred as fascial plane blocks, these aim to block the anterior cutaneous branches of the T2-T6 thoracic nerves. Pectointercostal fascial block (PIFB) is an effective technique for controlling sternal pain in heart surgeries where median sternotomy is performed.

    In cardiac surgeries performed with median sternotomy, mediastinal and thoracic tube placement sites are outside the area of effect of parasternal blocks, and sometimes the sternotomy incision extends below the T6 dermatome. Recto intercostal fascial plane block (RIFPB) has been defined as a complementary block for analgesia of this region. This study aims to evaluate the effectiveness of the combination of ultrasound-guided recto-intercostal fascial plane block and pectointercostal fascial block for postoperative analgesia management after open heart surgery (coronary artery bypass) with median sternotomy.

    Source : Importé depuis le centre

    Sites

    Centres participants

      1 centres
    • ISTANBUL MEDIPOL UNIVERSITY HOSPITAL

      Istanbul

      BAGCILAR, TURKEY (TÜRKIYE)

      Recrutement local
      État du recrutement: FERMÉ

    Dernière modification : 12 février 2026
    Données à jour depuis : 18 fév.
    Origine des données : clinicaltrials.gov
    Référence clinicaltrials.gov: NCT06285773