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The Impact of Esmolol Administration on Postoperative Recovery

NCT05567822 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 70

Last updated 2022-10-27

No results posted yet for this study

Summary

The aim of this study will be to investigate the effect of a continuous infusion of low dose esmolol on intraoperative and postoperative opioid consumption, as well as on postoperative recovery and chronic pain

Conditions

  • Pain, Acute
  • Pain, Postoperative
  • Pain, Chronic Post-Surgical
  • Esmolol
  • Inguinal Hernia Repair
  • Analgesia
  • Nociceptive Pain

Interventions

DRUG

Esmolol Hydrochloride

In the esmolol group, patients will receive a bolus dose of esmolol followed by a continuous infusion of esmolol intraoperatively

DRUG

normal saline

In the placebo group, patients will receive a bolus dose of normal saline followed by a continuous infusion of normal saline intraoperatively

Sponsors & Collaborators

  • Aretaieion University Hospital

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-10-01
Primary Completion
2024-10-01
Completion
2024-10-01

Countries

  • Greece

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05567822 on ClinicalTrials.gov