PORCzero: Reducing the Incidence of PostOperative Residual Curarization

Sponsor
Oscar Diaz-Cambronero (Other)
Overall Status
Unknown status
CT.gov ID
NCT03128151
Collaborator
Instituto de Investigacion Sanitaria La Fe (Other), INCLIVA (Industry)
3,000
6.4

Study Details

Study Description

Brief Summary

The NMB (Neuromuscular Blockade) is the most frequent complication in anesthesiology associated with an increase in adverse respiratory events in the postoperative period. Its appearance depends on multiple factors. The introduction of a comprehensive educational strategy aimed at promoting the proper management of NMB in the intraoperative period and a package of measures that must be performed (intraoperative neuromuscular monitoring and reversal of the effect of neuromuscular blockers) may contribute to a decrease in the incidence of NMB, Increase safety in the surgical patient and decrease associated costs.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Educational program for clinicians: implementation of a package of clinical prevention measures of NMB

Detailed Description

Multicenter, epidemiological, prospective, randomized, sequential study. The introduction of an educational program and a package of clinical measures (specific monitoring and pharmacological reversion) in the incidence of NMB will be evaluated by evaluating variations in this incidence of NMB, the rate of compliance with the preventive measures and the perception of the Safety in the perioperative, through pre and postoperative survey.

Study Design

Study Type:
Observational
Anticipated Enrollment :
3000 participants
Observational Model:
Case-Control
Time Perspective:
Prospective
Official Title:
PORCzero: PostOperative Residual Curarization
Anticipated Study Start Date :
Jun 20, 2018
Anticipated Primary Completion Date :
Dec 30, 2018
Anticipated Study Completion Date :
Dec 31, 2018

Arms and Interventions

Arm Intervention/Treatment
Study group

Intraoperative neuromuscular monitoring and pharmacological reversion according to data sheet

Behavioral: Educational program for clinicians: implementation of a package of clinical prevention measures of NMB
Intraoperative neuromuscular monitoring and pharmacological reversion of NMB according to data sheet

Control group

Treated according to usual clinical practice

Outcome Measures

Primary Outcome Measures

  1. Incidence of PORC. [Six months, first three months to evaluate PORC incidence and then three months to evaluate PORC incidence after educational intervention.]

    To reduce the incidence of PORC ≤ 10% by the introduction of an educational program and a bundle of preventive measures (including intraoperative monitoring and reversal of neuromuscular blocking agents (NMBA)).

Secondary Outcome Measures

  1. Compliance rate with the bundle of measures [Six months, first three months to evaluate PORC incidence and then three months to evaluate PORC incidence after educational intervention.]

    To evaluate if the educational program increases compliance of clinical preventive measures, if the reduction of incidence of BNMR is maintained, and, in addition, if this compliance is maintained over time.

  2. Rate of intraoperative monitoring [Six months, from the beginning, with no intervention, until the end of phase III (end of recruitment in both groups).]

    Rate of compliance of clinical prevention measures with intraoperative monitoring.

  3. Rate of reversal of NMBA [Six months, from the beginning, with no intervention, until the end of phase III (end of recruitment in both groups).]

    Rate of compliance of clinical prevention measures with NMBA reversal after surgery.

  4. Perception of safety -increase- by anesthesiologists [Six months, from the beginning, with no intervention, until the end of phase III (end of recruitment in both groups).]

    To evaluate, from the point of view of patient safety, whether the perception of safety by clinicians is maintained, through a survey before and after the intervention.

  5. Incidence of postoperative adverse events. [Six months, from the beginning, with no intervention, until the end of phase III (end of recruitment in both groups).]

    Incidence of postoperative complications in relation to the NMB reversal rate.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patients older than 18 years.

  • Classification of the American Society of Anesthesiologists (ASA I-III).

  • Patients with absence of cognitive deficit.

  • Informed informed consent prior to surgery

Exclusion Criteria:
  • Negative of the patient to participate in the study

  • Patients under the age of 18 or incapable of giving their consent

  • ASA IV-V

  • Pregnancy or breastfeeding

  • Associated neuromuscular disorders

  • Diabetes mellitus with diagnosed neuropathy

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Oscar Diaz-Cambronero
  • Instituto de Investigacion Sanitaria La Fe
  • INCLIVA

Investigators

  • Principal Investigator: Oscar Diaz Cambronero, MD, Hospital La Fe

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Oscar Diaz-Cambronero, Physician, specialist in Anesthesiology, Hospital Universitario La Fe
ClinicalTrials.gov Identifier:
NCT03128151
Other Study ID Numbers:
  • CEO-SUG-2016-01
First Posted:
Apr 25, 2017
Last Update Posted:
Jan 30, 2018
Last Verified:
Jan 1, 2018
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Oscar Diaz-Cambronero, Physician, specialist in Anesthesiology, Hospital Universitario La Fe
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 30, 2018