UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000004232 |
|---|---|
| Receipt number | R000005088 |
| Scientific Title | Preventing postoperative pain: Effect of Neurokinin-1 receptor antagonist |
| Date of disclosure of the study information | 2010/09/18 |
| Last modified on | 2010/09/18 17:35:51 |
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Basic information
Public title
Preventing postoperative pain: Effect of Neurokinin-1 receptor antagonist
Acronym
Preventing postoperative pain: Effect of Neurokinin-1 receptor antagonist
Scientific Title
Preventing postoperative pain: Effect of Neurokinin-1 receptor antagonist
Scientific Title:Acronym
Preventing postoperative pain: Effect of Neurokinin-1 receptor antagonist
Region
| Japan |
Condition
Condition
postoperative pain
Classification by specialty
| Anesthesiology |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
Evaluating the efficacy and tolerability of aprepitant for theprevention of the postoperative pain.
Basic objectives2
Safety,Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase
Not applicable
Assessment
Primary outcomes
postoperative pain and morphine consumption
Key secondary outcomes
frequency of the PONV and pruritus
Base
Study type
Interventional
Study design
Basic design
Parallel
Randomization
Randomized
Randomization unit
Blinding
Double blind -all involved are blinded
Control
Placebo
Stratification
Dynamic allocation
Institution consideration
Blocking
Concealment
Intervention
No. of arms
2
Purpose of intervention
Treatment
Type of intervention
| Medicine |
Interventions/Control_1
Patients received abdominal surgery of gynaecology are randomly assigned aprepitant group to Control group. On the day of surgery, aprepitant group takes orally Aprepitant (125mg) at 2 hours before induction of anesthesia.
Interventions/Control_2
Control group akes orally placebo (lactose powder capsule; 40 mg) at 2 hours before induction of anesthesia.
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
Patients are 20-65 years old who met the criteria of the American Society of Anesthesiologists physical status of 1-2 and undergo abdominal surgery. Having written informed consent.
Key exclusion criteria
Patiens are excluded the criteria of the American Society of Anesthesiologists physical status of over 3 and have the history of hypersensitivity for aprepitant.
Target sample size
95
Research contact person
Name of lead principal investigator
| 1st name | |
| Middle name | |
| Last name | Takashi Kawano |
Organization
Kochi Medical School Hospital
Division name
Anesthesiology
Zip code
Address
Kohasu, Oko, Nankoku City, Kochi 783-8505, Japan
TEL
Public contact
Name of contact person
| 1st name | |
| Middle name | |
| Last name |
Organization
Kochi Medical School Hospital
Division name
Anesthesiology
Zip code
Address
Kohasu, Oko, Nankoku City, Kochi 783-8505, Japan
TEL
Homepage URL
Sponsor or person
Institute
Department of Anesthesiology, Kochi Medical School Hospital
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
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
| 2010 | Year | 09 | Month | 18 | 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
Preinitiation
Date of protocol fixation
| 2010 | Year | 09 | Month | 18 | Day |
Date of IRB
Anticipated trial start date
| 2010 | Year | 09 | 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
| 2010 | Year | 09 | Month | 18 | Day |
Last modified on
| 2010 | Year | 09 | Month | 18 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000005088
