Errector Spinae Plane Block for Postoperative Pain Management in Cardiac Surgery: A Randomized Controlled Trial

N/AUnknownNCT04420104

Aydin Adnan Menderes University40 enrolled

Overview

The purpose of this study is to assess efficacy of erector spinae plane block (ESP) for postoperative pain management in cardiac surgery patients.

After being informed about the study and potential risks, all patients giving written informed consent will be randomised (single blind) as block group(patients is performed esp block) and control group. All patients will be evaluate during 48 hours for postoperative pain.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

SINGLE

Enrollment

Conditions

Erector Spinae Plane Block Cardiac Surgery

Interventions

erector spinae plane blockPROCEDURE

ESP Block: Bilateral ESP block and with ultrasound guidance will be applied A total 40 ml, 20 ml bupivacaine 0.5%, 20 ml saline.

iv analgesiaDRUG

iv contromal

Eligibility

Sex: ALLMin age: 18 YearsMax age: 85 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Must be ASA score I-III * Must be 18-75 years old * must undergo cardiac surgery Exclusion Criteria: * emergency surgery, * bleeding diathesis, * presence of contraindications to LA agents used in this study, * use of chronic opioids, * psychiatric disorders. * prolonged extubation * presence of infection at the injection site. * cardiovascular conditions (EF\<40, LMCA obstruction)

Locations (1)

Adnan Menderes University Medical Faculty, Anesthesiology and Reanimation Department

Aydin, Turkey (Türkiye)

RECRUITING

Outcomes

Primary Outcomes

change from baseline in pain the 10 point Visual Analog Scale (VAS) at hours 3,6,9,12,24,36,48.

The VAS is validated instrument assessing average pain. Possible scores range from 0 (no pain) to 10 (worst possible pain) Change= (hours 3,6,9,12,24,48 score- baseline)

Time frame: baseline and hours 3-6-12-24-36-48

time to mobilize the patient

time to mobilize the patient is reported as when the patient is mobilized

Time frame: Any time for 7 days

Central Contacts

Sinem Sari, Assoc Prof

CONTACT

90 507 539 63 13 sarisinem@yahoo.com

Data from ClinicalTrials.gov

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