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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03151369
Other study ID # 17-KAEK-007
Secondary ID
Status Completed
Phase N/A
First received April 18, 2017
Last updated February 19, 2018
Start date April 18, 2017
Est. completion date February 19, 2018

Study information

Verified date February 2018
Source Tokat Gaziosmanpasa University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The relationship between visual pain score and perfusion index in postoperative patients.


Description:

The patients' operated with general anesthesia and who had visual pain score(VAS) above 3 will be measured postoperatively perfusion index. .If the VAS score is above 3, 2 mg of morphine will be made. When the VAS score is below 3, the perfusion index will be measured again.Thus, the changes between vas and perfusion index will be measured.


Recruitment information / eligibility

Status Completed
Enrollment 89
Est. completion date February 19, 2018
Est. primary completion date January 20, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- Patients who underwent surgery with general anesthesia

Exclusion Criteria:

- Patients with caesarean section, pregnancy story and chronic pain

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Morphine
patients with the visual analog scale over 3 will receive morphine

Locations

Country Name City State
Turkey Gaziosmanpasa University Tokat

Sponsors (1)

Lead Sponsor Collaborator
Tokat Gaziosmanpasa University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Perfusion index Perfusion index Measurement of perfusion on the right ring finger two times in one day
Secondary visual analog scale measurement of pain intensity two times in one day
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