Fascial Plane Blocks In Cardiac Surgery
RecruitingNCT07622823
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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)
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.
Study details
- Official title
- The Effect Of Combined Rectus-Intercostal Fascial Plane Block Or Rectus Sheatf Block With A Pectoral-Intercostal Fascial Plane Block In Cardiac Surgery On Postoperative Opioid Consumption, Quality Of Recovery, And Chronic Pain: A Prospective, Observational Study
- Conditions
- Cardiovascular Surgery
- Regional Anaesthesia
- Postoperative Analgesia
- Interventions
- Other: PIFPB + RIFPB
- Other: PIFPB + RSB
- Other: Control
- Sponsor
- Antalya Health Sciences University
- Start date
- 2026-06-01
- Primary completion
- 2026-11-01
- Sex
- All
- Age range
- from 18 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: * elective cardiac surgery planned * over 18 years, adult * American Society of Anaesthesiology (ASA) score I-III Exclusion Criteria: * under 18 years of age, * ASA IV and above, * contraindications for the block application * history of cardiac surgery, * reoperated due to surgery-related complications after emergency surgery or postoperative elective surgery, * off-pump cardiac surgery or minimally invasive cardiac surgery * unable to be extubated in the intensive care unit at 24 hours postoperatively * history of chronic pain treatment * chronic alcoholism and substance abuse * declining to give written informed consent
Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT07622823