UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000019389
Receipt number R000022424
Scientific Title Evaluation of the Effect of intravenous paracetamol on perioperative pain in coronary artery bypass graft surgery
Date of disclosure of the study information 2015/11/16
Last modified on 2015/10/17 00:39:17

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Basic information

Public title

Evaluation of the Effect of intravenous paracetamol on perioperative pain in coronary artery bypass graft surgery

Acronym

Intravenous paracetamol and surgical pain

Scientific Title

Evaluation of the Effect of intravenous paracetamol on perioperative pain in coronary artery bypass graft surgery

Scientific Title:Acronym

Intravenous paracetamol and surgical pain

Region

Asia(except Japan)


Condition

Condition

Perioperative pain in coronary artery bypass graft surgery

Classification by specialty

Anesthesiology Cardiovascular surgery

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

1- Effects of paracetamol on perioperative pain

Basic objectives2

Others

Basic objectives -Others

1- perioperativr hemodynamic chakges
2- fever, nasea, vomiting
3- liver enzyme
4- opioid and sedative requirement

Trial characteristics_1

Confirmatory

Trial characteristics_2

Pragmatic

Developmental phase

Not applicable


Assessment

Primary outcomes

Preemptive administration of paracetamol and continue to be administered in the postoperative treatment with prescription of opioids drugs will improved quality of pain control after coronary artery bypass surgery.

Key secondary outcomes

1- the potency is not enough to reduce the need for narcotics and sedatives drugs and eliminate their side effects.
2- no additional liver damages
3- Hemodynamic stability


Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Double blind -all involved are blinded

Control

Placebo

Stratification

NO

Dynamic allocation

NO

Institution consideration


Blocking

NO

Concealment



Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Medicine

Interventions/Control_1

In paracetamol group 15 minutes before induction of anesthesia 1 g intravenous paracetamol in 50 cc normal saline solution was infused to the patient within 15 minutes.
Next dose of paracetamol was 1 g which was infused intravenously over 15 minutes within 6-4 hours after the first dose, so that the injection time was during the last 20 minutes of surgery.
Then subsequent doses of paracetamol, every 6 hours for 3 days was injected in intensive care at a rate of 1 g.

Interventions/Control_2

In the control group at all stages of paracetamol injection instead of paracetamol equal volume of normal saline was used.

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

40 years-old <

Age-upper limit

70 years-old >

Gender

Male and Female

Key inclusion criteria

Inclusion criteria for the study were: undergoing elective surgery CABG, the individual agreement to participate in the study, age 40 to 70 years, not having liver failure (Serum bilirubin greater than 1.8 mg per deciliter and aspartate and alanine aminotransfraz more than 1.5 times of the upper limit of normal), not having renal failure (serum creatinine greater than 2 mg per deciliter), not addictive to opioid drugs and psychotropic substances, and having cardiac ejection fraction greater than 30%.,

Key exclusion criteria

Excessive bleeding after surgery (more than 150 ml for the first two hours), having other surgeries in addition to coronary artery bypass surgery such as repair or replacement of heart valves, repeated surgery, and the need for aortic balloon support.

Target sample size

110


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Mojtaba Mansouri

Organization

Isfahan university of medical sciences

Division name

Anesthesiology and Critical Care Research Center, Department of Anesthesiology

Zip code


Address

Hezar Jarib st., Isfahan University of Medical Sciences, Isfahan, Iran.

TEL

+81-0989133101348

Email

mansouri@med.mui.ac.ir


Public contact

Name of contact person

1st name
Middle name
Last name Mojtaba mansouri

Organization

Isfahan university of medical sciences

Division name

Anesthesiology and Critical Care Research Center, Department of Anesthesiology

Zip code


Address

Hezar Jarib st., Isfahan University of Medical Sciences, Isfahan, Iran.

TEL

+81-098-9133101348

Homepage URL


Email

mansouri@med.mui.ac.ir


Sponsor or person

Institute

Isfahan university of medical sciences

Institute

Department

Personal name



Funding Source

Organization

---

Organization

Division

Category of Funding Organization

Outside Japan

Nationality of Funding Organization

Isfahan university of medical sciences


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 11 Month 16 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 10 Day

Date of IRB


Anticipated trial start date

2014 Year 01 Month 18 Day

Last follow-up date


Date of closure to data entry

2014 Year 07 Month 03 Day

Date trial data considered complete

2014 Year 07 Month 16 Day

Date analysis concluded

2014 Year 08 Month 04 Day


Other

Other related information



Management information

Registered date

2015 Year 10 Month 17 Day

Last modified on

2015 Year 10 Month 17 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000022424


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name