Use of Sildenafil Citrate in Management of Mild Pre-eclampsia
Pre-Eclampsia; Mild
About this trial
This is an interventional treatment trial for Pre-Eclampsia; Mild focused on measuring Mild pre-eclampsia Sildenafil Citrate
Eligibility Criteria
Inclusion Criteria:
- Uncomplicated mild pre-eclampsia; No clinical or investigatory findings suggestive severe pre-eclamptic toxemia.
- Gestational age of 28 - 36 weeks by good dates according to ACOG's - committee on obstetric practice - Method for Estimating Due Date (2014) who will receive the study's drug for at least one week before termination.
- Singleton viable pregnancy.
- Age: 18-35 years.
Exclusion Criteria:
- Severe pre-eclamptic toxemia (according to the NICE guidelines (2010): Hypertension in pregnancy: diagnosis and management)
- Intrauterine growth retardation.
- Use of medication that could interact with sildenafil citrate such as nitrates erythromycin, ketoconazole, itraconazole, antiretroviral agents and others.
- Presence of maternal co-morbidity disease as: DM, chronic hypertension, congestive heart failure, chronic kidney disease and SLE.
- Placenta previa.
- The patient is using aspirin.
The presence of a contraindication to the use of sildenafil citrate:
- Hypersensitivity to sildenafil citrate or any of the tablet ingredients.
- Patients with severe cardiovascular disease such as established cardiac failure and unstable angina pectoris.
- Previous episode of non-arteritic anterior ischaemic optic neuropathy.
- Severe hepatic impairment.
- Hypotension (blood pressure <90/50 mmHg).
- Hypertension (blood pressure >170/110 mmHg).
- Recent history of stroke or myocardial infarction.
- Known hereditary degenerative retinal disorders such as retinitis pigmentosa.
Sites / Locations
- Assiut Univeristy HospitalsRecruiting
Arms of the Study
Arm 1
Arm 2
Active Comparator
Placebo Comparator
Intervention Group
Control Group
• The intervention group will be supplied with Sildenafil Citrate (Respatio® 20mg tablets manufactured by Pharma Right Group , Egypt) according to the patient's weight by the rate of (1.5 mg/kg/day) divided into three doses per day ( every 8 hours) till termination of pregnancy.
- The control group will be supplied with a placebo drug that has the same shape, size and color but without the active ingredient and it would also be taken in a similar way. The placebo tablet will be manufactured at the faculty of pharmacy, Assiut University.