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PECs for Implantable Cardiac Electronic Device Insertion

Evaluation of the Efficacy of Pectoral Nerve (PECs) Blocks in Patients Undergoing Cardiac Implantable Electronic Device Insertion

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05528627
Enrollment
30
Registered
2022-09-06
Start date
2021-06-01
Completion date
2021-10-15
Last updated
2022-09-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Analgesia, Anesthesia, Cardiac Implantable Electronic Device, Nerve Block

Brief summary

The aim of this study is to evaluate the feasibility of the Pectoralis Nerve (PECS) block for CIED insertion.

Detailed description

Implantable Cardiac Electronic Device (CIED) insertion can be performed under local anesthesia, regional anesthesia, or general anesthesia. Novel regional blocks may improve pain management for such patients and can shorten their length of stay in the hospital. At the study, the investigators aimd to evaluate the efficacy and feasibility of the PECS block for CIED insertion procedure.

Interventions

OTHERPectoral Nerve (PECs) block

Pectoral Nerve (PECS) blocks were performed on the side of surgery, using the ultrasound-guided technique 30 min before the implantable cardiac electronic device (pacemaker, implantable cardioverter defibrillator) insertion procedure

Sponsors

Antalya Training and Research Hospital
Lead SponsorOTHER_GOV

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* American Society of Anaesthesiologists grade II-IV patients * in the age group of 18-80 years, * Patients undergoing CIED insertion

Exclusion criteria

* pre-existing infection at the block site, * coagulopathy, * morbid obesity (Body mass index \>35 kg m-2 ), * allergy to local anaesthetics, * decreased pulmonary reserve, * psychiatric illness

Design outcomes

Primary

MeasureTime frameDescription
amount of intraoperative additional local anesthetic1 houramount of intraoperative additional local anesthetic administered by the cardiologist during the CIED insertion procedure was recorded.
number of patients who requiring intraoperative additional local anesthetic1 hourNumber of patients requiring intraoperative additional local anesthetic was recorded.

Secondary

MeasureTime frameDescription
Postoperative pain scores24 hoursPostoperative pain scores were assessed by Visual Analogue Scale (VAS) scores from 0 (no pain) to 10 (maximum possible pain) for 24 hours postoperatively.
time to first postoperative analgesic requirement24 hourstime to first postoperative analgesic requirement was recorded for 24 hours postoperatively
patient satisfaction24 hoursPatient satisfaction was assessed by a 5-point Likert scale (ie, 1: very dissatisfied, 2: dissatisfied, 3: neutral, 4: satisfied, and 5: very satisfied) 24 hours after the procedure
cardiologist satisfaction24 hoursCardiologist satisfaction was assessed by a 5-point Likert scale (ie, 1: very dissatisfied, 2: dissatisfied, 3: neutral, 4: satisfied, and 5: very satisfied) 24 hours after the procedure

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026