Analgesic efficacy of a regional technique (erector spinae plane block) following scoliosis surgery.

Phase 1

• Conditions: Postoperative pain following scoliosis surgery; Therapeutic area: Analytical, Diagnostic and Therapeutic Techniques and Equipment [E] - Anesthesia and Analgesia [E03]

• Registration Number: EUCTR2021-004506-21-ES
• Lead Sponsor: Hospital Universitario Fundación Alcorcón

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2021-10-19
• Last Update Posted: 6 December 2021

Recruitment & Eligibility

• Status: Authorised-recruitment may be ongoing or finished
• Sex: All
• Target Recruitment: 40

Inclusion Criteria

- Patients older than 16 years old
- Elective scoliosis surgery involving more than 4 spaces
- ASA I-III
- Primary surgery and reinterventions
- Idiopathic and degenerative scoliosis
Are the trial subjects under 18? yes
Number of subjects for this age range: 10
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range 10
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range 20

Exclusion Criteria

- Urgent surgery
- Infection in the site of surgery
- Allergy to any of the drugs used in the study.
- Patient refusal
- Absence of informed consent
- Surgical complication that prevents an adequate follow up (i.e. hemorrhage, delirium, etc.)

Study & Design

• Study Type: Interventional clinical trial of medicinal product
• Study Design: Not specified