UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000005753 |
|---|---|
| Receipt number | R000006803 |
| Scientific Title | Comparisons of postoperative pain intensity between laparoscopy and laparotomy in early-stage uterine endometrial cancer. |
| Date of disclosure of the study information | 2011/06/10 |
| Last modified on | 2015/07/23 10:58:17 |
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Basic information
Public title
Comparisons of postoperative pain intensity between laparoscopy and laparotomy in early-stage uterine endometrial cancer.
Acronym
Comparisons of postoperative pain intensity between laparoscopy and laparotomy in early-stage uterine endometrial cancer.
Scientific Title
Comparisons of postoperative pain intensity between laparoscopy and laparotomy in early-stage uterine endometrial cancer.
Scientific Title:Acronym
Comparisons of postoperative pain intensity between laparoscopy and laparotomy in early-stage uterine endometrial cancer.
Region
| Japan |
Condition
Condition
early-stage uterine endometrial cancer
Classification by specialty
| Obstetrics and Gynecology |
Classification by malignancy
Malignancy
Genomic information
NO
Objectives
Narrative objectives1
The purpose of this study is to compare the postoperative pain intensity between laparoscopy and laparotomy for
early-stage uterine endometrial cancer.
Basic objectives2
Efficacy
Basic objectives -Others
Trial characteristics_1
Confirmatory
Trial characteristics_2
Pragmatic
Developmental phase
Assessment
Primary outcomes
Postoperative pain intensity using Numerical Rating Scale (NRS) until no analgesia is required.
Key secondary outcomes
Hospital stay.
Base
Study type
Interventional
Study design
Basic design
Single arm
Randomization
Non-randomized
Randomization unit
Blinding
Open -no one is blinded
Control
Historical
Stratification
Dynamic allocation
Institution consideration
Blocking
Concealment
Intervention
No. of arms
1
Purpose of intervention
Treatment
Type of intervention
| Maneuver |
Interventions/Control_1
Intervention 1: laparoscopic surgery
Control 1: laparotomy
Interventions/Control_2
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
| 70 | years-old | >= |
Gender
Female
Key inclusion criteria
Preoperative diagnosis;
Endometrioid adenocarcinoma of the uterine corpus, grade 1,
FIGO stage 1a,
neither operative nor anesthesia risk
Key exclusion criteria
All patients except for endometrioid adenocarcinoma of the uterine corpus, grade 1, or FIGO stage 1a.
Target sample size
5
Research contact person
Name of lead principal investigator
| 1st name | |
| Middle name | |
| Last name | Hiroshi Tatsumi |
Organization
Kyoto prefectural university of medicine
Division name
Department of obstetrics and gynecology
Zip code
Address
465 Kajii-cho, Kawaramachi-Hirokoji, Kamigyo-ku, Kyoto
TEL
075-251-5560
htatsumi@koto.kpu-m.ac.jp
Public contact
Name of contact person
| 1st name | |
| Middle name | |
| Last name | Hiroshi Tatsumi |
Organization
Kyoto prefectural university of medicine
Division name
Department of obstetrics and gynecology
Zip code
Address
465 Kajii-cho, Kawaramachi-Hirokoji, Kamigyo-ku, Kyoto 602-8566, JAPAN
TEL
075-251-5560
Homepage URL
htatsumi@koto.kpu-m.ac.jp
Sponsor or person
Institute
Kyoto prefectural university of medicine
Institute
Department
Personal name
Funding Source
Organization
University hospital, Kyoto prefectural university of medicine
Organization
Division
Category of Funding Organization
Self funding
Nationality of Funding Organization
Japan
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
京都府立医科大学附属病院（京都府）
Other administrative information
Date of disclosure of the study information
| 2011 | Year | 06 | Month | 10 | 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
Open public recruiting
Date of protocol fixation
| 2011 | Year | 05 | Month | 10 | Day |
Date of IRB
Anticipated trial start date
| 2011 | Year | 07 | Month | 01 | Day |
Last follow-up date
| 2013 | Year | 12 | Month | 01 | Day |
Date of closure to data entry
| 2013 | Year | 12 | Month | 01 | Day |
Date trial data considered complete
| 2014 | Year | 02 | Month | 01 | Day |
Date analysis concluded
| 2014 | Year | 03 | Month | 01 | Day |
Other
Other related information
Management information
Registered date
| 2011 | Year | 06 | Month | 10 | Day |
Last modified on
| 2015 | Year | 07 | Month | 23 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000006803
