Ultrasound Guided Sacral Erector Spina Plane Block as a Main Anesthetic Method

Ultrasound Guided Sacral Erector Spina Plane Block as a Main Anesthetic Method: Single Center Experience

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT05674006

Acronym

ESP

Enrollment

Registered

2023-01-06

Start date

2023-01-25

Completion date

2023-03-16

Last updated

2023-03-17

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

Conditions

Anesthesia, Local

Keywords

Anesthesia, ESP, Sacral

Brief summary

The goal of this retrospective observational study is to demonstrate investigators' experience of Ultrasound guided Sacral Erector Spina Plane Block as an anesthetic technique in patients underwent sacral plastic and reconstructive surgeries. The main question\[s\] it aims to answer are: * block indication, level * results, side effects and complications

Detailed description

Erector Spina Plane Block is an interfascial plane block that is performed by injecting the local anesthetic solution between transverse process of the vertebra and erector spina muscle. It is found to be an inexpensive,easily applied, effective and safe technique for chronic pain.(1) Ultrasound guided Erector Spina Plane Block(ESP) is getting more and more widely used for analgesia and as an anesthetic technique.(2,3) Regional anesthesia techniques provide safer, more stable and advantageous anesthetic management, especially in high-risk patients. Ultrasound guided Sacral ESP is described by Tulgar et all.in 2019 and can be used either for analgesia or as an anesthetic technique. (4) In this retrospective study investigators planed to demonstrate one year of experience of this block for sacral plastic and reconstructive surgery. Demographic data of patients who underwent sacral surgery with sacral ESP block, indication of block, level of block, drug dose concentration, effect, side effect and results that were recorded will be analyzed.

Interventions

None listed

Study design

Observational model

COHORT

Time perspective

RETROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Inclusion criteria

* being going for a sacral surgery * American Society of Anesthesiology status (ASA) 1 - 4

Exclusion criteria

* emergency * ASA-5

Design outcomes

Primary

Measure	Time frame	Description
Block success	up to 1 year	Effectiveness of Sacral Erector Spinae Plane Block as an Anesthetic technique

Secondary

Measure	Time frame	Description
Number and amount of required perioperative analgesic/anesthetic drugs	up to 2 hours	The number and amount of drugs administered will be determined from the anesthesia file records when the patient feels pain or shows dissatisfaction with anesthesia.

Countries

Turkey (Türkiye)

Outcome results