Erector Spinae Plane Block With Two Different Volume for Open Heart Surgery

Ultrasound Guided Erector Spinae Plane Block With Two Different Volume for Open Heart Surgery: Randomized Controlled Study

Status

UNKNOWN

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT04989933

Acronym

ESP

Enrollment

Registered

2021-08-04

Start date

2021-08-02

Completion date

2021-11-01

Last updated

2021-08-04

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

Conditions

Sternotomy Pain

Brief summary

The erector spine plane block is currently used in many surgeries to provide postoperative analgesia. It has also been used successfully in open-heart surgery for postoperative sternotomy pain. However, an ideal volume that will provide optimum analgesia has not yet been determined. This study aims to compare the effects of ESP block administered in two different volumes on poststernotomy pain.

Interventions

PROCEDUREUltrasound-guided erector spinae plane block

Ultrasound-Guided erector spinae plane block with 0.25% bupivacaine

Study design

Allocation

RANDOMIZED

Intervention model

PARALLEL

Primary purpose

PREVENTION

Masking

DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender

ALL

Age

18 Years to 65 Years

Healthy volunteers

Inclusion criteria

* American Society of Anesthesiologist's physiologic state I-III patients Undergoing Open Heart Surgery

Exclusion criteria

* chronic pain bleeding disorders renal or hepatic insufficiency patients on chronic non-steroidal anti-inflammatory medications emergency cases

Design outcomes

Primary

Measure	Time frame	Description
Rescue analgesia	Post-extubation 24 hours	Total amount of rescue analgesic

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026