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Analgesia in Patients Undergoing Transfemoral Transcatheter Aortic Valve Implantation (TF-TAVI) (TF-TAVI)

Primary Purpose

Aortic Valve Stenosis

Status
Completed
Phase
Not Applicable
Locations
Poland
Study Type
Interventional
Intervention
Nerve block
Local infiltration
TAVI
Additional intraoperative analgesia
Additional postoperative analgesia
Sponsored by
Medical University of Gdansk
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Aortic Valve Stenosis focused on measuring Ilioinguinal Iliohypogastric nerve block, local anaesthesia infiltration, ultrasound-guided, pain control

Eligibility Criteria

65 Years - undefined (Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • patients with aortic valve stenosis referred for TF-TAVI
  • using a minimalist approach of local anesthesia or nerve block with conscious sedation

Exclusion Criteria:

  • patient's refusal to participate
  • allergy to local anaesthetic
  • TF-TAVI requiring general anesthesia or surgical cut-down
  • patients with major cognitive impairment and inability to assess their pain level in Numerical Rating Scale (NRS).

Sites / Locations

  • University Clinical Centre

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Nerve block

Local infiltration

Arm Description

ultrasound-guided ilioinguinal iliohypogastric nerve block performed by the anaesthesiologist for Transaortic valve implantation (TAVI) insertion with eventual additional intraoperative analgesia (AIA) and/or additional postoperative analgesia (APA)

local anaesthesia infiltration performed by the operator for TAVI insertion with eventual intraoperative additional analgesia (AIA) and/or postoperative analgesia (APA)

Outcomes

Primary Outcome Measures

Numeric Rating Scale (NRS)
The numeric rating scale will be used to determine the intraoperative and postoperative pain intensity levels of the patients. Pain intensity is scored 0-10 (0=no pain, 10=the worst pain imaginable). The pain intensity will be measured at 5 time points intraoperatively (femoral artery cannulation, aortic valve system introduction, aortic valve system removal, vessel closure devices insertion and the end of the operation) and at 2 time intervals postoperatively (0-12 hours and 12-24 hours).

Secondary Outcome Measures

Additional intraoperative analgesia consumption
Fentanyl and paracetamol consumption during the operation.
Additional postoperative analgesia consumption
Oxycodone and paracetamol consumption in first 24 hours after the operation
Patient satisfaction with analgesia
Categorical quantification: Yes / No
Intraoperative and postoperative cost calculations
Sum of anesthetics and analgesics administered during operation and within first 24 hours after operation

Full Information

First Posted
August 10, 2018
Last Updated
January 14, 2020
Sponsor
Medical University of Gdansk
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1. Study Identification

Unique Protocol Identification Number
NCT03863899
Brief Title
Analgesia in Patients Undergoing Transfemoral Transcatheter Aortic Valve Implantation (TF-TAVI)
Acronym
TF-TAVI
Official Title
Pain Control With Ultrasound-guided Ilioinguinal Iliohypogastric Nerve Block Compared With Local Anesthesia Infiltration in Patients Undergoing Transfemoral Transcatheter Aortic Valve Implantation (TF-TAVI): a Prospective, Randomized Trial
Study Type
Interventional

2. Study Status

Record Verification Date
January 2020
Overall Recruitment Status
Completed
Study Start Date
July 2, 2018 (Actual)
Primary Completion Date
December 31, 2019 (Actual)
Study Completion Date
December 31, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Medical University of Gdansk

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Ilioinguinal and iliohypogastric (ILIH) nerve blocks are frequently performed for analgesia in inguinal surgery. The investigators hypothesized that preoperative ultrasound-guided ilioinguinal and iliohypogastric (ILIH) nerve blocks will produce better intraoperative analgesia and less analgesic requirement postoperatively in comparison to commonly used preoperative local infiltration anaesthesia for patients undergoing transfemoral transcatheter aortic valve implantation (TF-TAVI).
Detailed Description
It is a prospective, randomized trial. The patients will be randomized to one of the 2 groups: Group 1 - NERVE BLOCK. Ultrasound-guided ILIH nerve block will be performed by attending anaesthesiologist. Group 2 - LOCAL INFILTRATION. Local anaesthetic infiltration of the operative area will be performed by operator. During surgery patients will receive low-dose propofol infusion in order to achieve conscious sedation level, when indicated. An extra dose of local anaesthetic drug for infiltration of the surgical field or intravenous fentanyl or/and intravenous paracetamol will be given as rescue analgesics in patients reporting pain sensation. The patients will be observed for 24 hours. The pain at rest will be assessed using numeric rating scale (NRS 0 -10; 0 = no pain: 10 = max pain imaginable). On the first postoperative day intravenous analgesics will be given on demand (paracetamol 1 g iv (if NRS <5) and oxycodone 2,5 mg iv (if NRS > or = 5)).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Aortic Valve Stenosis
Keywords
Ilioinguinal Iliohypogastric nerve block, local anaesthesia infiltration, ultrasound-guided, pain control

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
100 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Nerve block
Arm Type
Experimental
Arm Description
ultrasound-guided ilioinguinal iliohypogastric nerve block performed by the anaesthesiologist for Transaortic valve implantation (TAVI) insertion with eventual additional intraoperative analgesia (AIA) and/or additional postoperative analgesia (APA)
Arm Title
Local infiltration
Arm Type
Active Comparator
Arm Description
local anaesthesia infiltration performed by the operator for TAVI insertion with eventual intraoperative additional analgesia (AIA) and/or postoperative analgesia (APA)
Intervention Type
Procedure
Intervention Name(s)
Nerve block
Other Intervention Name(s)
Ultrasound-guided ilioinguinal iliohypogastric nerve block
Intervention Description
drug mixture: 10-15 ml 0.5% ropivacaine plus 5 ml 1% lidocaine plus 1 mg dexamethasone plus 50 ug adrenaline
Intervention Type
Procedure
Intervention Name(s)
Local infiltration
Other Intervention Name(s)
Local anesthesia infiltration
Intervention Description
15-20 ml of mixture of 0.5% bupivacaine and 1% lidocaine (1:1)
Intervention Type
Procedure
Intervention Name(s)
TAVI
Other Intervention Name(s)
Transaortic valve implantation
Intervention Description
Insertion of an aortic valve prothesis through the aorta accessed through femoral artery
Intervention Type
Drug
Intervention Name(s)
Additional intraoperative analgesia
Other Intervention Name(s)
AIA
Intervention Description
Administration of any analgesics during the operation
Intervention Type
Drug
Intervention Name(s)
Additional postoperative analgesia
Other Intervention Name(s)
APA
Intervention Description
Administration of any analgesics within first 24 hours after the operation
Primary Outcome Measure Information:
Title
Numeric Rating Scale (NRS)
Description
The numeric rating scale will be used to determine the intraoperative and postoperative pain intensity levels of the patients. Pain intensity is scored 0-10 (0=no pain, 10=the worst pain imaginable). The pain intensity will be measured at 5 time points intraoperatively (femoral artery cannulation, aortic valve system introduction, aortic valve system removal, vessel closure devices insertion and the end of the operation) and at 2 time intervals postoperatively (0-12 hours and 12-24 hours).
Time Frame
24 hours
Secondary Outcome Measure Information:
Title
Additional intraoperative analgesia consumption
Description
Fentanyl and paracetamol consumption during the operation.
Time Frame
24 hours
Title
Additional postoperative analgesia consumption
Description
Oxycodone and paracetamol consumption in first 24 hours after the operation
Time Frame
24 hours
Title
Patient satisfaction with analgesia
Description
Categorical quantification: Yes / No
Time Frame
3 days
Title
Intraoperative and postoperative cost calculations
Description
Sum of anesthetics and analgesics administered during operation and within first 24 hours after operation
Time Frame
1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: patients with aortic valve stenosis referred for TF-TAVI using a minimalist approach of local anesthesia or nerve block with conscious sedation Exclusion Criteria: patient's refusal to participate allergy to local anaesthetic TF-TAVI requiring general anesthesia or surgical cut-down patients with major cognitive impairment and inability to assess their pain level in Numerical Rating Scale (NRS).
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Romuald Lango, MD, PhD
Organizational Affiliation
Department of Cardiac Anaesthesiolgy UCC of Gdansk
Official's Role
Study Chair
Facility Information:
Facility Name
University Clinical Centre
City
Gdańsk
ZIP/Postal Code
80-211
Country
Poland

12. IPD Sharing Statement

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Analgesia in Patients Undergoing Transfemoral Transcatheter Aortic Valve Implantation (TF-TAVI)

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