Pain Evaluation of Venous Cannulation to Predict Postoperative Pain

Prediction of Postoperative Pain From Individually Assessed Pain Intensity Levels Associated With Venous Cannulation

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT02982109

Enrollment

600

Registered

2016-12-05

Start date

2017-02-27

Completion date

2017-05-22

Last updated

2019-04-04

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

Conditions

Pain, Postoperative

Brief summary

The investigators have recently reported a relationship between pain induced by peripheral venous cannulation and postoperative pain. The purpose of this study is to validate this method of postoperative pain prediction in a larger cohort subjected to different types of surgery.

Detailed description

* The investigators will study all adult (\>18 years old) patients going through surgery at the site during a defined period of time. Before induction of anesthesia participants will be asked to assess (in VAS units) the pain intensity associated with peripheral venous cannulation. The maximum level of postoperative pain intensity will be recorded in the post-anesthesia care unit. * After the endpoint of the study, the patient records will be reviewed, and de-identified relevant data be recorded and analyzed in the Statistical Package for the Social Sciences (SPSS) software. * Sample size assessment: In a previous study patients scoring ≥ 2.0 on venous cannulation assessed their median pain postoperatively at 5.8 VAS units compared with 2.9 in those scoring \< 2.0 - corresponding to a difference in maximum postoperative pain intensity of almost three VAS units. To statistically confirm, with unpaired non-parametric tests, 80 % power (β), and 95% probability (1- α), half of that difference (1.5 VAS units) in pain intensity level between patients scoring above or below 2.0 VAS units, respectively, would require 55 patients in each group subjected to the same kind of surgery. With 4 groups of cases and controls 440 patients would need to be included. As the study is strictly observational, 600 patients will be included to make up for possible missing data. * Statistics: The Mann-Whitney U- test will be used to compare differences in postoperative pain intensity levels, and the Pearson Chi-square test to compare proportions of patients with moderate or severe postoperative pain, in patients differing in pain scores (above or below 2.0 VAS units) on venous cannulation. Logistic regression analysis will be used to adjust for gender and age and to evaluate the predictive ability of proposed method.

Interventions

None listed

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to 80 Years

Healthy volunteers

Inclusion criteria

* 18-80 years old * Scheduled for surgery in Halmstad * Prepared for surgery in the preoperative ward or ward 71 (day-case or direct admittance)

Exclusion criteria

* Inability to handle the Visual Analog Scale * Hospitalized already before surgery

Design outcomes

Primary

Measure	Time frame	Description
Maximum postoperative pain intensity (0.0-10.0 VAS units)	2 hours after surgery	Patients scoring their pain associated with venous cannulation to \<2 VAS units will be compared to patients scoring ≥2 VAS units considering median level of maximum postoperative pain intensity.

Secondary

Measure	Time frame	Description
Risk of developing moderate to severe postoperative pain	2 hours after surgery	Proportion of patients with moderate or severe (≥4 VAS units) postoperative pain will be compared between groups of patients scoring \</≥ 2 VAS units on peripheral venous cannulation.
Influence of gender	2 hours after surgery	With logistic regression analysis investigate the potential influence of gender on the predictive ability of this test.

Countries

Sweden

Outcome results