UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000012624 |
|---|---|
| Receipt number | R000014763 |
| Scientific Title | Comparison of different doses of parecoxib for the prevention of postanesthetic shivering. |
| Date of disclosure of the study information | 2013/12/19 |
| Last modified on | 2013/12/19 11:36:20 |
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Basic information
Public title
Comparison of different doses of parecoxib for the prevention of postanesthetic shivering.
Acronym
Parecoxib and shivering
Scientific Title
Comparison of different doses of parecoxib for the prevention of postanesthetic shivering.
Scientific Title:Acronym
Parecoxib and shivering
Region
| Asia(except Japan) |
Condition
Condition
patients undergoing general anesthesia were recruited into the study
Classification by specialty
| Anesthesiology |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
To compare the efficacy of different doses of parecoxib administered intraoperatively on postoperative shivering
Basic objectives2
Safety,Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
the overall incidence and grades of postoperative shivering
Key secondary outcomes
Base
Study type
Interventional
Study design
Basic design
Parallel
Randomization
Randomized
Randomization unit
Individual
Blinding
Double blind -all involved are blinded
Control
Active
Stratification
Dynamic allocation
Institution consideration
Blocking
Concealment
Intervention
No. of arms
3
Purpose of intervention
Prevention
Type of intervention
| Medicine |
Interventions/Control_1
In group P40, intravenous parecoxib (40mg) was given following the induction of anesthesia.
Interventions/Control_2
In group P20, intravenous parecoxib (20mg) was given following the induction of anesthesia.
Interventions/Control_3
In group S, intravenous normal saline was given following the induction of anesthesia.
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
| 60 | years-old | >= |
Gender
Male and Female
Key inclusion criteria
adult patients (ASA physical status I or II) scheduled for elective minor urological surgery under general anesthetic with no prior medication were included in this study
Key exclusion criteria
1, initial body temperature more than 38 centigrade or less than 36.5 centigrade;
2, hyperthyroidism, hypertension, diabetes mellitus, impaired renal or liver functions, endocrine or cardiopulmonary disease;
3, taking vasoactive or antidepressant drugs, receiving intraoperative blood or blood products transfusion;
4, known history of alcohol or substance abuse, or possible pregnancy;
Target sample size
120
Research contact person
Name of lead principal investigator
| 1st name | |
| Middle name | |
| Last name | Chen jie |
Organization
Third Military Medical University
Division name
Department of Anaesthesiology, Southwest Hospital,
Zip code
Address
Gaotanyan road, Shapingba, Chongqing, China
TEL
+81-086-23-68754197
cjandsh@tmmu.edu.cn
Public contact
Name of contact person
| 1st name | |
| Middle name | |
| Last name | Chen jie |
Organization
Third Military Medical University
Division name
Department of Anaesthesiology, Southwest Hospital,
Zip code
Address
Gaotanyan road, Shapingba, Chongqing, China
TEL
+81-086-23-68754197
Homepage URL
cjandsh2009@yahoo.cn
Sponsor or person
Institute
Department of Anaesthesiology, Southwest Hospital,
Institute
Department
Personal name
Funding Source
Organization
Department of Anaesthesiology, Southwest Hospital,
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
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
| 2013 | Year | 12 | Month | 19 | 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
Enrolling by invitation
Date of protocol fixation
| 2013 | Year | 12 | Month | 16 | Day |
Date of IRB
Anticipated trial start date
| 2014 | Year | 01 | Month | 13 | 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
| 2013 | Year | 12 | Month | 19 | Day |
Last modified on
| 2013 | Year | 12 | Month | 19 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000014763
