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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03807960
Other study ID # pci
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 1, 2019
Est. completion date June 21, 2019

Study information

Verified date July 2019
Source Tokat Gaziosmanpasa University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study is aimed to show the effect of information method on properly usage of the patient controlled analgesia(PCA) device


Description:

Postoperative pain is still a challenge for anesthesiologist. Patient controlled analgesia is an effective method for postoperative pain management. However, most of the patient can not use the device properly. The important cause of inabilities about device usage is insufficient information.In the patient information, visual, oral or written communication methods can be chosen. However, which method is suitable for our patient group is not clear.This study is aimed to show the effect of information method on properly usage of the patient controlled analgesia(PCA) device


Recruitment information / eligibility

Status Completed
Enrollment 96
Est. completion date June 21, 2019
Est. primary completion date June 20, 2019
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- informed consent

- Elective hysterectomy

Exclusion Criteria:

- Opioid abuse or Chronic opioid usage

- opioid allergy

- obesity(BMI>30)

- psychiatric disease

- more than American Anesthesiologist Score 2

Study Design


Related Conditions & MeSH terms


Intervention

Other:
written form
The written form which include PCA usage information.
video
The video about PCA usage
routine care
The routine description about PCA usage

Locations

Country Name City State
Turkey Gaziosmanpasa University Hospital Tokat Merkez

Sponsors (2)

Lead Sponsor Collaborator
Tugba Karaman Tokat Gaziosmanpasa University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Other Length of stay hospital Number of the day that patients stay at hospital will be recorded. Up to the postoperative 10 days
Primary Pain Score Numeric rating scale (0 to 10) will be used for postoperative pain score At postoperative 24th hours.
Secondary Postoperative analgesic consumption Total opioid dosage will be recorded Up to the postoperative 24th hours.
Secondary PCA device usage The number of demand dose During postoperative 24 hours
Secondary PCA device demand dose duration The duration of the patients' demanding dose During postoperative 24hours
Secondary Patient's satisfaction The numeric rating scale (0 to 10) will be used. In this scale 0 will be the worst, 10 will be the best satisfaction. At the postoperative 24th hours
Secondary The change of the postoperative pain score Numeric rating scale (0 to 10) will be used to evaluate the pain score. The change in this score during postoperative 24 hours will be calculated.(the first score will be extracted from the last score) Up to the postoperative 24th hours.
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