UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000016800
Receipt number R000019371
Scientific Title Investigation into safety of preoperative oral intake of carbohydrate rich beverage in diabetic patients. Part2
Date of disclosure of the study information 2015/03/31
Last modified on 2018/03/18 12:21:50

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Basic information

Public title

Investigation into safety of preoperative oral intake of carbohydrate rich beverage in diabetic patients. Part2

Acronym

Preoperative oral intake of carbohydrate rich beverage in diabetic patients. Pert2

Scientific Title

Investigation into safety of preoperative oral intake of carbohydrate rich beverage in diabetic patients. Part2

Scientific Title:Acronym

Preoperative oral intake of carbohydrate rich beverage in diabetic patients. Pert2

Region

Japan


Condition

Condition

Diabetic patients undergoing surgery with general anesthesia

Classification by specialty

Anesthesiology

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

They say preoperative oral intake of carbohydrate rich beverage improves preoperative thirst, hunger and insulin resistance. But in diabetic patients hyperglycemia induced by oral intake of carbohydrate rich beverage was concerned. And so we examined the safety of preoperative oral intake of carbohydrate rich beverage in diabetic patients.

Basic objectives2

Safety

Basic objectives -Others


Trial characteristics_1

Confirmatory

Trial characteristics_2

Pragmatic

Developmental phase

Not applicable


Assessment

Primary outcomes

Blood glucose level after induction of anesthesia.

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

No treatment

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Food

Interventions/Control_1

Group A: Type 2 diabetes patients were not permitted to take solid food from 2100 hours the day before surgery, permitted to drink clear fluid and encouraged to drink carbohydrate rich beverage (Arginaid Water) until 700 hours the day of surgery. After induction of general anesthesia, radial arterial catheter was inserted and blood gas analysis was done.
From September 2012 to April 2014, Data were collected in the study registered UMIN000011266.

Interventions/Control_2

Group C: Type 2 diabetes patients were not permitted to take solid food from 2100 hours the day before surgery, permitted to drink clear fluid. After induction of general anesthesia, radial arterial catheter was inserted and blood gas analysis was done. From January 2011 to September 2012, data were collected in medical records retrospectively.

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

100 years-old >

Gender

Male and Female

Key inclusion criteria

Patients with type 2 diabetes mellitus who underwent surgery with general anesthesia entering the operating room at 845 hours.

Key exclusion criteria

Type 1 diabetes mellitus
Final stage of a terminal illness
Untreated diabetes
Uncontrolled diabetes
Unconsciousness
Emergency surgeries
Cardiac surgeries

Target sample size

54


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Motoi Sasuga

Organization

Tokyo Metropolitan Tama Medical Center

Division name

Department of anesthesiology

Zip code


Address

2-8-29 Musashidai, Fuchu, Tokyo 183-8524, Japan

TEL

042-323-5111

Email

motoi_sasuga@tmhp.jp


Public contact

Name of contact person

1st name
Middle name
Last name Motoi Sasuga

Organization

Tokyo Metropolitan Tama Medical Center

Division name

Department of anesthesiology

Zip code


Address

2-8-29 Musashidai, Fuchu, Tokyo 183-8524, Japan

TEL

042-323-5111

Homepage URL


Email

motoi_sasuga@tmhp.jp


Sponsor or person

Institute

Department of anesthesiology, Tokyo Metropolitan Tama Medical Center

Institute

Department

Personal name



Funding Source

Organization

none

Organization

Division

Category of Funding Organization

Self funding

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 03 Month 31 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 01 Month 18 Day

Date of IRB


Anticipated trial start date

2015 Year 04 Month 01 Day

Last follow-up date


Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2015 Year 03 Month 14 Day

Last modified on

2018 Year 03 Month 18 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000019371


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name