Transversus Abdominis Plane Block Versus Erector Spina Plane Block

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

100 participants

Study Classification

INTERVENTIONAL

Study Start Date

2019-10-01

Study Completion Date

2020-01-01

Brief Summary

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Regional anesthesia and analgesia techniques are frequently used to provide pain control in pediatric surgical applications. The main advantages of these techniques include ease of application, good analgesic efficacy and low risk of complications (1). It reduces the need for parenteral opioids and increases the quality of postoperative pain control and the satisfaction of the patient and family (2). The aim of this study was to compare the contribution of TAP block and ESP block combined with sedation in pediatric surgery to anesthesia and analgesia during surgery without general anesthesia.

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Detailed Description

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Conditions

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Intraoperative Pain Control

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Investigators

Study Groups

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transversus abdominis plane block

Group 1 (n: 50): those who underwent TAP block after induction of propofol atropine and maintained with only 1 mg / kg / h propofol in anesthesia maintenance

Group Type ACTIVE_COMPARATOR

Ultrasound guided erector spinae block

Intervention Type DEVICE

Group 2 (n: 50): those who underwent ESP block after propofol atropine induction and maintained with only 1 mg / kg / h propofol in anesthesia maintenance

erector spinae block

Group 2 (n: 50): those who underwent ESP block after propofol atropine induction and maintained with only 1 mg / kg / h propofol in anesthesia maintenance

Group Type ACTIVE_COMPARATOR

Ultrasound guided erector spinae block

Intervention Type DEVICE

Group 2 (n: 50): those who underwent ESP block after propofol atropine induction and maintained with only 1 mg / kg / h propofol in anesthesia maintenance

Interventions

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Ultrasound guided erector spinae block

Group 2 (n: 50): those who underwent ESP block after propofol atropine induction and maintained with only 1 mg / kg / h propofol in anesthesia maintenance

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* ASA I-II,
* undergo elective lower abdominal surgery
* 2-6 years

Exclusion Criteria

* Psychiatric patients,
* weight\> 40 kg,
* those with cardiac-pulmonary-neurological disease,
* those with bleeding disorders,
* infection or wound scarring at the injection site,
* known allergy to local anesthetics

Minimum Eligible Age

2 Years

Maximum Eligible Age

6 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No