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Trial registered on ANZCTR
Registration number
ACTRN12614000808640
Ethics application status
Approved
Date submitted
8/07/2014
Date registered
30/07/2014
Date last updated
30/07/2014
Type of registration
Retrospectively registered
Titles & IDs
Public title
Can treatment of unexplained recurrent abortion patients with nitric oxide donors decrease the incidence of abortion?
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Scientific title
Comparative study between folic acid control group and folic acid plus isosorbid mononitrate as a nitric oxide donors study group treatment of unexplained recurrent abortion patients as regards incidence of abortion
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Secondary ID [1]
284936
0
Nil
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Unexplained recurrent abortion
292417
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Condition category
Condition code
Reproductive Health and Childbirth
292732
292732
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0
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Fertility including in vitro fertilisation
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
A control of 30 patients with unexplained recurrent abortion treated with folic acid 0.5 mg once daily orally starting before pregnancy until 20 weeks gestation and a study group of 30 patients treated with folic acid 0.5 mg once daily orally plus isosorbid mononitrate 20 mg dailly applied vaginally
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Intervention code [1]
289764
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Treatment: Drugs
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Comparator / control treatment
Control group treated with folic acid 0.5 mg orally from before pregnancy to 20 weeks gestation
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Control group
Active
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Outcomes
Primary outcome [1]
292582
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Incidence of abortion in both groups
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Assessment method [1]
292582
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Timepoint [1]
292582
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20 weeks gestation
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Primary outcome [2]
292583
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Uterine artery resistance and pulsation indices before treatment and at 20 weeks gestation after treatment measured by trans-vaginal and trans-abdominal pulsed color Doppler ultrasound
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Assessment method [2]
292583
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Timepoint [2]
292583
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20 weeks gestation
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Secondary outcome [1]
309261
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Nil
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Assessment method [1]
309261
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Timepoint [1]
309261
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Nil
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Eligibility
Key inclusion criteria
Patients with unexplained recurrent abortion with normal uterine cavity, normal glucose tolerance, normal levels of antiphospholipid antibodies, normal thyroid functions and normal karyotyping
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Minimum age
20
Years
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Maximum age
30
Years
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Sex
Females
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Can healthy volunteers participate?
No
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Key exclusion criteria
Patients treated with vasodilators
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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Masking / blinding
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Who is / are masked / blinded?
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Intervention assignment
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Other design features
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Phase
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Type of endpoint/s
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
1/01/2013
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Actual
1/01/2013
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Date of last participant enrolment
Anticipated
1/12/2013
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Actual
1/12/2013
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
60
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Accrual to date
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Final
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Recruitment outside Australia
Country [1]
6201
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Egypt
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State/province [1]
6201
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Funding & Sponsors
Funding source category [1]
289564
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Hospital
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Name [1]
289564
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Benha university hospital
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Address [1]
289564
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Kalyuopia, Benha, Farid Nada street,
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Country [1]
289564
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Egypt
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Primary sponsor type
Hospital
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Name
Benha university hospital
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Address
Kalyoupia , Benha, Farid Nada street
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Country
Egypt
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Secondary sponsor category [1]
288352
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None
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Name [1]
288352
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Address [1]
288352
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Country [1]
288352
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Ethics approval
Ethics application status
Approved
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Summary
Brief summary
The study included a control and a study group each 30 cases with history of unexplained recurrent abortion. The control group was treated with folic acid tablet 0.5 mg once daily orally and the study group treated with folic acid plus isosorbid mononitrate 20 mg given vaginally. Treatment was given monthly from day 21-23 of the cycle until menstruation and continued if pregnancy occurred until 20 weeks gestation. Doppler ultrasound was done vaginally before treatment and abdominally at 20 weeks gestation to measure uterine artery resistance and pulsation indices. Patients were treated until 20 weeks gestation to compare uterine artery indices before and after treatment and the incidence of abortion in both groups
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
49770
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Prof Mohamed Abdelrazik
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Address
49770
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Department of Obstetrics and Gynecology, Benha Faculty of Medicine, Benha, Farid Nada street
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Country
49770
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Egypt
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Phone
49770
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+20 02 26070837 or +20 013 3225385
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Fax
49770
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Email
49770
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[email protected]
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Contact person for public queries
Name
49771
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Mohamed Abdelrazik
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Address
49771
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Department of Obstetrics and Gynecology, Benha Faculty of Medicine, Benha, Farid Nada street
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Country
49771
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Egypt
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Phone
49771
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+20 02 26070837 or +20 013 3225385
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Fax
49771
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Email
49771
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[email protected]
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Contact person for scientific queries
Name
49772
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Mohamed Abdelrazik
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Address
49772
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Department of Obstetrics and Gynecology, Benha Faculty of Medicine, Benha, Farid Nada street
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Country
49772
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Egypt
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Phone
49772
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+20 02 26070837 or +20 013 3225385
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Fax
49772
0
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Email
49772
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[email protected]
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No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
No additional documents have been identified.
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