Health TrialsbyHealthPanel

Fascial Plane Blocks In Cardiac Surgery

ConditionsCardiovascular SurgeryRegional AnaesthesiaPostoperative Analgesia
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorAntalya Health Sciences University

About this trial

The aim of the present study is to evaluate the effects of the recto-intercostal fascial plane block (RIFPB) or the rectus sheath block (RSB) combined with the pectoral-intercostal fascial plane block (PIFPB) on postoperative analgesia in patients undergoing cardiac surgery.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

elective cardiac surgery planned

over 18 years, adult

American Society of Anaesthesiology (ASA) score I-III

Disqualifiers

under 18 years of age,

ASA IV and above,

contraindications for the block application

history of cardiac surgery,

Trial population

It is planned to include ASA score I-IIII adult patients who are scheduled to elective cardiac surgery

Trial design

Design model

Case-only

Time perspective

Prospective

Treatments tested in this trial

  • PIFPB + RIFPB

    Other intervention

    The procedure is performed under ultrasound guidance in a separate regional anaesthesia room during the preoperative period, under standard ASA monitoring.

  • PIFPB + RSB

    Other intervention

    The procedure is performed under ultrasound guidance in a separate regional anaesthesia room during the preoperative period, under standard ASA monitoring.

  • Control

    Other intervention

    Regional anesthesia is not applied.

Treatment groups

90 Participants
are divided into 3 treatment groups
Group A: PIFPB+RIFPB1 intervention
Group B: PIFPB+RSB1 intervention
Group C: Control1 intervention

Trial outcomes

Primary outcomes

1

postoperative opioid consumption

Time frame
48 hours

Secondary outcomes

1

postoperative recovery quality

TThe Quality of Recovery-15 (QoR-15) is a 15-question questionnaire validated to assess poetoperative recovery. This questionnaire assesses patients' pain, physical comfort, physical independence, psychological support, and emotional status in the erly postoperative period. The patient is asked to express their status scoring from 0 to 10; therefore, the total score ranges from 0 to 150 points.

Time frame
24 hours
2

postoperative pain scores

The NRS score (0=no pain; 10=most severe pain) will be used to assess postoperative pain

Time frame
48 hours
3

chronic pain

Patients will be telephoned 3 months after the operation and the presence, localization, and intensity of the pain, its character, and its relation with rest and/or activity will be recorded by asking only verbally. The NRS score (0=no pain; 10=most severe pain) will be used to assess postoperative pain.

Time frame
3 months

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Antalya Health Sciences University

Lead sponsor

Source ClinicalTrials.gov
Apply now