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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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TCTR |
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Last refreshed on:
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29 April 2024 |
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Main ID: |
TCTR20151011001 |
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Date of registration:
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11/10/2015 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Effect of single rectal dose of Misoprostol prior to abdominal hysterectomy in women with symptomatic leiomyoma: a randomized double blind clinical trial
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Scientific title:
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Effect of single rectal dose of Misoprostol prior to abdominal hysterectomy in women with symptomatic leiomyoma: a randomized double blind clinical trial |
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Date of first enrolment:
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01/10/2015 |
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Target sample size:
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40 |
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Recruitment status: |
Active, not recruiting |
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URL:
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https://www.thaiclinicaltrials.org/show/TCTR20151011001 |
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Study type:
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Interventional |
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Study design:
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Randomized
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Phase:
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Phase 3
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Countries of recruitment
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iran
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Contacts
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Name:
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pouria
yazdian |
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Address:
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yazd
8853721121
yazd
iran |
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Telephone:
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09385101025 |
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Email:
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pouria_yazdian_a@yahoo.com |
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Affiliation:
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student research committee, shahid sadoughi university of medical sciences |
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Name:
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pouria
yazdian |
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Address:
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yazd
8853721121
yazd
iran |
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Telephone:
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09385101025 |
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Email:
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pouria_yazdian_a@yahoo.com |
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Affiliation:
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student research committee, shahid sadoughi university of medical sciences |
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Key inclusion & exclusion criteria
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Inclusion criteria: uterine myoma
candidate for abdominal hysterectomy
Exclusion criteria: emergency condition
Age minimum:
0 Years
Age maximum:
0 Years
Gender:
Female
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Health Condition(s) or Problem(s) studied
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Misoprostol
bleeding volume
abdominal hysterectomy
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abdominal hysterectomy
bleeding volume
Misoprostol
Misoprostol
bleeding volume
abdominal hysterectomy
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Intervention(s)
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400 micrograms rectal Misoprostol was administered to cases 30 minutes prior to operation. ,The controls received placebo in return.
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Experimental Drug,Placebo Comparator Drug
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intervention roup,control
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Primary Outcome(s)
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bleeding 0 litr
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Secondary Outcome(s)
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age 0 year
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Source(s) of Monetary Support
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none
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Ethics review
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Status:
Approval date:
Contact:
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Results
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Results available:
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Date Posted:
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Date Completed:
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10/10/2015 |
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URL:
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