CompletedNot Applicable

RIB for Perioperative Analgesia in CIED Patients

Turkey (Türkiye)53 participantsStarted 2024-06-04

Plain-language summary

Rhomboid intercostal plane block (RIB) has been described in the last decade. Various clinical applications have been found to provide hemithorax analgesia. The use of cardiac implantable electronic devices (CIEDs) is increasing due to comorbidities in the elderly population. Increased myocardial stress with pain in these patients may increase the frequency of adverse cardiac events. Therefore, perioperative pain management ensures patient welfare, reduces complications, and maintains stable hemodynamic values. In this study, we aimed to evaluate the outcomes of RIB in terms of perioperative analgesia and patient and physician satisfaction in patients undergoing CIED.

Who can participate

Age range18 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * over 18 years of age, * no previous ICD or Pacemaker implantation attempt * ASA ( American Society of Anesthesiologists ) score of 2-3, * INR \< 2.0 , * Signing the volunteer consent form, * Patients who met the study criteria will be included in the study. Exclusion Criteria: * Morbidly obese patients (BMI\>35 kg/m2), * Advanced decompensated heart failure with New York Heart Association (NYHA) stage 4, * Having severe chronic obstructive pulmonary disease, * Allergy to the prescribed medications , * Those who have a skin infection or lesion in the area to be blocked, * Cannot be communicated and cannot be given a position, * Severe psychosis and progressive neurological deficits and muscle disease, * ICD/ Pacemaker revision or upgrade to be made, * ICD battery replacement * Pregnant patients will be excluded from the study.

What they're measuring

The pain will be assessed by the Numeric Rating Scale-11(NRS -11). Minimum pain score is point zero, maximum pain score is ten points.

Timeframe: 4 months

Investigation patient and physician satisfaction assessed by 5-point Likert scale. One point represents strongly unsatisfied and 5 points represent strongly satisfied.

Timeframe: 4 months

Trial details

NCT IDNCT06449599

SponsorIstanbul University - Cerrahpasa

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2024-10-15

View on ClinicalTrials.gov More Anesthesia trials

Plain-language summary

Who can participate

Age range18 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

What they're measuring

The pain will be assessed by the Numeric Rating Scale-11(NRS -11). Minimum pain score is point zero, maximum pain score is ten points.

Timeframe: 4 months

Investigation patient and physician satisfaction assessed by 5-point Likert scale. One point represents strongly unsatisfied and 5 points represent strongly satisfied.

Timeframe: 4 months