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Completed

NCT Number: NCT02143128

Efficacy Side-effect Score (ESS): Development and Evaluation of a New Tool for Patients After Surgery

We hypothesized that better control of postoperative pain treatment and its side effects by monitoring ESS might influence the degree of mobility and morbidity in surgical patients and consequently reduce LOS. Thus, our aim was to validate the influence of recording ESS and the application of a "call-out algorithm" on LOS in two university hospitals in which the routine policy of registration of pain had not been adopted yet.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Astana University Hospital, Astana, Astana, Kazakhstan

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About this study

Using clinical experience and consensus-methodology the investigators picked up and digitalized information about mental, postoperative nausea, vomiting and pain status at the rest and during mobilization in so called Efficacy Safety Score (ESS). Depending on expression of patient's complaints, all mentioned above clinical features are scored. We hypothesized that better control of postoperative pain treatment and its side effects by monitoring ESS might influence the degree of mobility and morbidity in surgical patients and consequently reduce length of hospital stay (LOS). Thus, our aim was to validate the influence of recording ESS and the application of a "call-out algorithm" on LOS in two university hospitals in which the routine policy of registration of pain had not been adopted yet. The primary endpoint of the study was to assess LOS in groups of patients with different types of clinical data records and "call-out algorithms," while secondary endpoints were to compare the degree of mobilization, number of postoperative nonsurgical complications, and 28-day survival between the groups.and summarized in the total score.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • All adult postoperative patients that are inpatients, and scheduled for hospitalization for more than 8 hours

Exclusion criteria

  • Children, mental illness, communication difficulties

Treatment and study plan

Efficacy Safety Score

Other

Evaluation using the score for postoperative patients

Other names: ESS

Verbal Numeric Rating Scale

Other

Patients assessed for postoperative pain using VNRS (0-10)

Other names: VNRS

Primary outcomes

  1. Length of Hospital Stay (LOS)

    Time frame: 28 days

    Assess LOS in groups of patients with different types of clinical data records an "all-out algorithms"

Sponsors and collaborators

Lead sponsor

Vestre VikenHF Kongsberg Sykehus

Other

Collaborators

  • Norwegian Medical Association

Registry information

Official study title

Safety and Quality for Inpatients After Surgery at the Ward. Development and Evaluation of a New Tool: Efficacy Side-effect Score (ESS)

Acronym: ESScore

Important dates

Study start
2014
Primary completion
2015
Study completion
2015
First posted
May 20, 2014
Registry last updated
Sep 11, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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