Analgesic Effectiveness Of Ultrasound-Guided Transversus Abdominis Plan (TAP) Block In Transcatheter Aortic Valve Implantation (TAVI)

Status: Recruiting
Location: See location...
Intervention Type: Device, Procedure
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Hemodynamic stability is the main goal of the anesthetic method during TAVI. Pain during the procedure may cause patients to move therefore hemodynamic instability. This may lead to undesirable complications for the patient and the physician. At the same time, it may affect the process quality and cause the processing time to be extended. In this prospective-randomised study, ultrasound-guided transversus abdominis plan block will be performed to reduce pain. We aimed to contribute to the reduction of undesirable outcomes for the patient and physician by providing adequate anesthesia with TAP block accompanied by sedation, and to present its impact on the quality of the healthcare service provided by evaluating patient and physician satisfaction.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• TAVI procedures

• over 18 years of age

• INR \< 1,5

• elective procedures

• Signing the volunteer consent form

• Providing optimal images in ultrasound imaging

Locations
Other Locations
Turkey
Istanbul University-Cerrahpaşa
RECRUITING
Istanbul
Contact Information
Primary
Ayla Esin
ayla.esin@iuc.edu.tr
+905326343959
Backup
Kerem Erkalp, professor
+905327879500
Time Frame
Start Date: 2024-12-28
Estimated Completion Date: 2025-06-30
Participants
Target number of participants: 50
Treatments
Active_comparator: Block group
Local anesthesia and sedation will be applied as standard procedure and unilateral USG-guided TAP block will be performed. In both groups, an additional dose of anesthetic drugs (midazolam 0.05mg/kg and fentanyl 1mcg/kg or propofol 0.5-1mg/kg) will be administered slowly IV when the patient feels pain, wakes up (BIS\>80) or moves.
Sham_comparator: Control group
Local anesthesia and sedation will be applied as standard procedure in the control group (C) (n: 25). In both groups, an additional dose of anesthetic drugs (midazolam 0.05mg/kg and fentanyl 1mcg/kg or propofol 0.5-1mg/kg or ) will be administered slowly IV when the patient feels pain, wakes up (BIS\>80) or moves
Sponsors
Leads: Istanbul University - Cerrahpasa

This content was sourced from clinicaltrials.gov