Sildenafil in Sever Intrauterine Growth Retardation (IUGR)
Primary Purpose
Intra-Uterine Growth Retardation
Status
Completed
Phase
Not Applicable
Locations
Egypt
Study Type
Interventional
Intervention
treatment
Placebo
Sponsored by
About this trial
This is an interventional other trial for Intra-Uterine Growth Retardation
Eligibility Criteria
Inclusion Criteria:
• pregnancy complicated by severe IUGR [abdominal circumference (AC)< 5th percentile] the gestational age <25 weeks or an estimate of the fetal weight was <600 gm (excluding known fetal anomaly/syndrome and/or planned termination) ( von Dadelszen.et al;2011).
Exclusion Criteria:
- known aneuploid anomaly, syndrome congenital infection.
- If there is a plan to terminate the pregnancy.
Sites / Locations
- Beni-Suef University
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
Intervention group
Control group
Arm Description
women with severe IUGR
women with severe IUGR
Outcomes
Primary Outcome Measures
Umbilical artery Pulsatility index
Change in umbilical artery pulsatility index after medication
Middle cerebral artery Pulsatility index
Change in middle cerebral artery pulsatility index after medication
fetal abdominal circumference growth velocity
proportion of women in each group for whom fetal AC growth velocity will change post randomization.
Secondary Outcome Measures
Rate of drug side effects
Women in the Sildenafil-treated group will be also monitored for adverse side-effects, such as flushing, lightheadedness and visual disturbance
Birth weight
weight of neonate at birth in grams
Full Information
NCT ID
NCT03153215
First Posted
May 5, 2017
Last Updated
July 6, 2018
Sponsor
Beni-Suef University
Collaborators
Cairo University
1. Study Identification
Unique Protocol Identification Number
NCT03153215
Brief Title
Sildenafil in Sever Intrauterine Growth Retardation
Acronym
IUGR
Official Title
Evaluation of Addition of Sildenafil Citrate for Treatment of Severe Intrauterine Growth Restriction
Study Type
Interventional
2. Study Status
Record Verification Date
July 2018
Overall Recruitment Status
Completed
Study Start Date
May 6, 2017 (Actual)
Primary Completion Date
December 31, 2017 (Actual)
Study Completion Date
December 31, 2017 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Beni-Suef University
Collaborators
Cairo University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Severe fetal growth restriction (FGR) complicates approximately 0.4% of pregnancies and severely increases the risk of perinatal morbidity and mortality.Sildenafil citrate may offer a potential therapeutic strategy to improve uteroplacental blood flow in IUGR pregnancies.
Detailed Description
The aim of our study is to evaluate the effect of sildenafil citrate therapy on severe early and late onset intrauterine growth retardation.A total of 46 patients with severe early onset intrauterine growth retardation will be enrolled in a prospective case control study .
Patients will randomly be allocated to two groups with 23 patients in each group.Sildenafil citrate therapy may increase the likelihood of increased growth velocity [measured by abdominal circumference (AC) (ultrasound)] for fetuses of pregnancies complicated by severe early-onset IUGR .Sildenafil is a potent and selective inhibitor of cGMP-specific phosphodiesterase type 5 (PDE5), which is responsible for degradation of cGMP which results in increased levels of cGMP, leading to smooth muscle relaxation. Placental disease, consequent on deficient uteroplacental blood flow, includes FGR, pre-eclampsia, and placental abruption and has been implicated in more than 50% of iatrogenic premature births .For this reason, the problem of severe FGR forms a substantial portion of the population that tertiary care centres care.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Intra-Uterine Growth Retardation
7. Study Design
Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
A total of 46 patients with severe early onset intrauterine growth retardation will be enrolled in a randomized placebo control controlled study .
Patients will randomly be allocated to two groups with 23 patients in each group
Masking
ParticipantInvestigator
Masking Description
Patients will randomly be allocated to two groups with 23 patients in each group
Allocation
Randomized
Enrollment
46 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Intervention group
Arm Type
Active Comparator
Arm Description
women with severe IUGR
Arm Title
Control group
Arm Type
Active Comparator
Arm Description
women with severe IUGR
Intervention Type
Other
Intervention Name(s)
treatment
Intervention Description
We will offer Sildenafil citrate (20 mg per os three times daily until delivery) as innovative therapy to 23 women with severe IUGR ('Sildenafil-treated') in addition to fish oil and zinc supplementation.
Intervention Type
Other
Intervention Name(s)
Placebo
Intervention Description
Placebo tablets similar to Sildenafil will be given to control group in addition to fish oil and zinc supplementation.
Primary Outcome Measure Information:
Title
Umbilical artery Pulsatility index
Description
Change in umbilical artery pulsatility index after medication
Time Frame
between 24 gestational weeks until 36 weeks
Title
Middle cerebral artery Pulsatility index
Description
Change in middle cerebral artery pulsatility index after medication
Time Frame
between 24 gestational weeks until 36 weeks
Title
fetal abdominal circumference growth velocity
Description
proportion of women in each group for whom fetal AC growth velocity will change post randomization.
Time Frame
between 24 gestational weeks until 36 weeks
Secondary Outcome Measure Information:
Title
Rate of drug side effects
Description
Women in the Sildenafil-treated group will be also monitored for adverse side-effects, such as flushing, lightheadedness and visual disturbance
Time Frame
between 24 and 36 gestational weeks
Title
Birth weight
Description
weight of neonate at birth in grams
Time Frame
between 24 and 36 gestational weeks
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
25 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
• pregnancy complicated by severe IUGR [abdominal circumference (AC)< 5th percentile] the gestational age <25 weeks or an estimate of the fetal weight was <600 gm (excluding known fetal anomaly/syndrome and/or planned termination) ( von Dadelszen.et al;2011).
Exclusion Criteria:
known aneuploid anomaly, syndrome congenital infection.
If there is a plan to terminate the pregnancy.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Nesreen A Shehata, MD
Organizational Affiliation
Beni-Suef University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Beni-Suef University
City
Cairo
State/Province
Beni-Suef
ZIP/Postal Code
12412
Country
Egypt
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
17014813
Citation
Ananth CV, Vintzileos AM. Maternal-fetal conditions necessitating a medical intervention resulting in preterm birth. Am J Obstet Gynecol. 2006 Dec;195(6):1557-63. doi: 10.1016/j.ajog.2006.05.021. Epub 2006 Oct 2.
Results Reference
background
PubMed Identifier
24007710
Citation
Lausman A, Kingdom J; MATERNAL FETAL MEDICINE COMMITTEE. Intrauterine growth restriction: screening, diagnosis, and management. J Obstet Gynaecol Can. 2013 Aug;35(8):741-748. doi: 10.1016/S1701-2163(15)30865-3. English, French.
Results Reference
background
PubMed Identifier
11594552
Citation
Lee MJ, Conner EL, Charafeddine L, Woods JR Jr, Del Priore G. A critical birth weight and other determinants of survival for infants with severe intrauterine growth restriction. Ann N Y Acad Sci. 2001 Sep;943:326-39. doi: 10.1111/j.1749-6632.2001.tb03813.x.
Results Reference
background
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Sildenafil in Sever Intrauterine Growth Retardation
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