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Erector Spinae Plane Block for Post-Operatory Analgesia in Cardiac Surgery: a Randomized Clinical Trial

Erector Spinae Plane Block for Post-Operatory Analgesia in Cardiac Surgery: a Randomized Clinical Trial

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
REBEC
Registry ID
RBR-9djgjv
Enrollment
Unknown
Registered
2020-11-03
Start date
2020-06-01
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Anesthesia for cardiac surgery, post operative pain.

Interventions

The study has 2 groups (the intervention x control). Each group has 24 pacients. All patients will be monitored with pulse oximetry, electrocardiography, invasive blood pressure, capnography and anest
E01.370.600.550.324
E03.091

Sponsors

Santa Casa de Belo Horizonte
Lead Sponsor
Santa Casa de Belo Horizonte
Collaborator

Eligibility

Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: All patients above 18 years old; who will be submitted to cardiac surgeries at Santa Casa de Belo Horizonte; after sign the consent term.

Exclusion criteria

Exclusion criteria: Pacientes under 18 years old. Patients with active bleeding or with coagulation disturbances. Shocked patients. Patients waiting for heart transplantation. People with insuficient data for analisys or who decline the consent term.

Design outcomes

Primary

MeasureTime frame
We expect opioid consumption reduction in those pacients who received the block. We will assess the pain scale and administrate morfine if necessary.

Secondary

MeasureTime frame
We expect fast recovery, faster postoperatory extubation, reduction in intensive care unit stay and faster hospital discharge, reduction of postoperatory infection rates and mortality rates.

Countries

Brazil

Contacts

Public ContactMagda Fernandes
fernandesmagda21@gmail.com+5531992171956

Outcome results

None listed

Source: REBEC (via WHO ICTRP)