UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000015683
Receipt number R000018135
Scientific Title The comparison of the indicator of oxycodone administration during thyroidectomy operation: surgical pleth index versus conventional vital sign
Date of disclosure of the study information 2015/08/11
Last modified on 2015/08/11 17:00:09

* This page includes information on clinical trials registered in UMIN clinical trial registed system.
* We don't aim to advertise certain products or treatments


Basic information

Public title

The comparison of the indicator of oxycodone administration during thyroidectomy operation: surgical pleth index versus conventional vital sign

Acronym

The comparison of the indicator of oxycodone administration during thyroidectomy

Scientific Title

The comparison of the indicator of oxycodone administration during thyroidectomy operation: surgical pleth index versus conventional vital sign

Scientific Title:Acronym

The comparison of the indicator of oxycodone administration during thyroidectomy

Region

Asia(except Japan)


Condition

Condition

Patients who are undergoing elective thyroidectomy

Classification by specialty

Surgery in general Anesthesiology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

The aims of this study are to evaluate the effectiveness of surgical pleth index-guided analgesia compared with conventional practice analgesia in the aspects of intraoperative anesthetic and analgesic requirement, hemodynamic change, recovery profiles and postoperative pain, analgesic requirement in adult whose age are from 20 to 65.

Basic objectives2

Safety

Basic objectives -Others


Trial characteristics_1

Confirmatory

Trial characteristics_2

Pragmatic

Developmental phase

Not applicable


Assessment

Primary outcomes

Intraoperative analgesic requirement

Key secondary outcomes

Intraoperative anesthetic consumption, hemodynamics, recovery profiles, and postoperative pain, analgesic requirement


Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Double blind -all involved are blinded

Control

Active

Stratification

NO

Dynamic allocation

NO

Institution consideration


Blocking

YES

Concealment



Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Device,equipment

Interventions/Control_1

Intravenous oxycodone 1mg will be administered when surgical pleth index (SPI) value is above 50 in SPI group for 1 min. Time intervalof administration is minimum 5min .

Interventions/Control_2

Intravenous oxycodone 1mg will be administered when blood pressure or heart rate is increased to above 20% of the baseline value in control group for 1 min. Time intervalof administration is minimum 5min .

Interventions/Control_3


Interventions/Control_4


Interventions/Control_5


Interventions/Control_6


Interventions/Control_7


Interventions/Control_8


Interventions/Control_9


Interventions/Control_10



Eligibility

Age-lower limit

20 years-old <=

Age-upper limit

65 years-old >=

Gender

Male and Female

Key inclusion criteria

Adult patients aged 20-65 years with a physical status of 1 (the American Society of Anesthesiologists rating) who are scheduled to undergo elective thyroidectomy.

Key exclusion criteria

Patients with a history of cardiovascular, respiratory (asthma), neurologic (seizure), kidney, liver disease, mood disorder, prematurity, or developmental delay, the presence of upper respiratory infection, hypersensitivity to drugs, and those receiving analgesics, sedatives or psychiatric medication will be excluded.

Target sample size

92


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Young ju Won

Organization

Guro Hospital, Korea University College of Medicine

Division name

Department of Anesthesiology and Pain Medicine

Zip code


Address

148 Gurodong-ro, Guro-gu, Seoul, Korea

TEL

82-2-2626-1437

Email

moma2@naver.com


Public contact

Name of contact person

1st name
Middle name
Last name Young ju Won

Organization

Guro Hospital, Korea University College of Medicine

Division name

Department of Anesthesiology and Pain Medicine

Zip code


Address

148 Gurodong-ro, Guro-gu, Seoul, Korea

TEL

82-2-2626-1437

Homepage URL


Email

moma2@naver.com


Sponsor or person

Institute

Korea University

Institute

Department

Personal name



Funding Source

Organization

Korea University

Organization

Division

Category of Funding Organization

Outside Japan

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization


Address


Tel


Email



Secondary IDs

Secondary IDs

NO

Study ID_1


Org. issuing International ID_1


Study ID_2


Org. issuing International ID_2


IND to MHLW



Institutions

Institutions



Other administrative information

Date of disclosure of the study information

2015 Year 08 Month 11 Day


Related information

URL releasing protocol


Publication of results

Unpublished


Result

URL related to results and publications


Number of participants that the trial has enrolled


Results


Results date posted


Results Delayed


Results Delay Reason


Date of the first journal publication of results


Baseline Characteristics


Participant flow


Adverse events


Outcome measures


Plan to share IPD


IPD sharing Plan description



Progress

Recruitment status

Completed

Date of protocol fixation

2014 Year 11 Month 25 Day

Date of IRB


Anticipated trial start date

2014 Year 11 Month 26 Day

Last follow-up date


Date of closure to data entry

2015 Year 03 Month 13 Day

Date trial data considered complete

2015 Year 03 Month 16 Day

Date analysis concluded

2015 Year 05 Month 01 Day


Other

Other related information



Management information

Registered date

2014 Year 11 Month 13 Day

Last modified on

2015 Year 08 Month 11 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000018135


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name