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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02826746
Other study ID # AJIRB-MED-CT4-16-089
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 2016
Est. completion date March 2019

Study information

Verified date April 2019
Source Ajou University School of Medicine
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The primary purpose of this study is to investigate the effect of intravenous magnesium on postoperative throat pain after thyroidectomy.

The secondary purpose of this study is to investigate the effect of intravenous magnesium on total dose of fentanyl in recovery room after thyroidectomy.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date March 2019
Est. primary completion date March 2019
Accepts healthy volunteers No
Gender Female
Age group 20 Years to 85 Years
Eligibility Inclusion Criteria:

- Thyroidectomy

Exclusion Criteria:

- Allergy to magnesium

- Chronic pain

- Chronic opioid use

- Chronic NSAID use

- Renal dysfunction

- Liver dysfunction

- Cardiac arrythmia

- Seizure

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Magnesium Sulfate
adminstration of intravenous magnesium as bolus of 50 mg/kg, followed by continuous infusion at rate of 10 mg/kg/h
Normal saline
the same bolus and infusion volumes of normal saline

Locations

Country Name City State
Korea, Republic of Department of Anesthesiology and Pain Medicine, Ajou University School of Medicine Suwon Seoum

Sponsors (1)

Lead Sponsor Collaborator
Ajou University School of Medicine

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Throat pain pain assessment using visual analog scale Up to 48 hours after surgery end
Secondary Fentanyl dose in recovery room Up to 30 minutes after surgery end
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