Could Algometric Assessment be Effective to Adjust Postoperative Analgesic Requirement?

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

80 participants

Study Classification

INTERVENTIONAL

Study Start Date

2012-02-29

Study Completion Date

2015-05-31

Brief Summary

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The purpose of this study is to determine the correlation between preoperative algometer score and the amount of postoperative analgesic consumption. The algometer score of the patients will be recorded in the preoperative period. In postoperative period, the analgesic consumption rate will record and compare with the algometer score.

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Detailed Description

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The aim of this study is to define the correlation between preoperative algometer score and the analgesic consumption rate. A total of 80 patients whose undergo septoplasty or septorhinoplasty will be included in this study. After preoperative examination, a positive pressure using algometer device will be performed until minimal pain is felt. In postoperative period, the amount of analgesic consumption of the patient will record and compare with the algometer score.

Conditions

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Pain

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

SCREENING

Blinding Strategy

NONE

Study Groups

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Algometer

Algometer used patients

Group Type OTHER

Algometer

Intervention Type DEVICE

Algometer performed patients

Interventions

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Algometer

Algometer performed patients

Intervention Type DEVICE

Other Intervention Names

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J-Tech Commander - Algometer

Eligibility Criteria

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Inclusion Criteria

* Patients those undergo septoplasty or septorhinoplasty

Exclusion Criteria

* Hypertension
* Diabetes mellitus type 1 or 2
* Continuous use of analgesics
* Patients whose do not accept to participate in the study
* Patients those reoperated for bleeding

Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes