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Effect of Sildenafil Citrate on Uteri- Placental Perfusion, Doppler Indices in Growth Restricted Fetuses

A

Al Hayat National Hospital

Status

Completed

Conditions

Pregnancy Complication

Treatments

Other: placebo
Drug: sildenafil citrate

Study type

Interventional

Funder types

Other

Identifiers

NCT02362399
menoufia ob/gyn 1

Details and patient eligibility

About

To detect the effect of sildenafil citrate on Doppler parameters in fetuses suffering from growth restriction to support its use later as prolonged therapy in those pregnancies at higher risk for such complication.

Full description

Participants were randomized in 1:1 ratio into one of the following drug regime:

Group (I): "sildenafil citrate group" This group consisted of 22 women who received single oral dose of 50 mg sildenafil citrate.

Group (II): "placebo group" This group consisted of 22 women who received single oral dose of placebo. All participants were evaluated by ultrasound once they admitted and again after 2-hours following administration of either of the treatment tablets. One sonographer was allocated to evaluate all mothers included in the study.

Enrollment

54 patients

Sex

Female

Ages

18 to 45 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Patients were admitted to the study based on the following inclusion criteria:

  1. Any age and any party.
  2. Body mass index between 25 and 35.
  3. Singleton pregnancy.
  4. Gestational age of 24 weeks or more. Gestational age was established on the basis of menstrual dates and confirmed by first or second trimester ultrasound for booked patients, however, if a difference of > 7 days or > 10 days during first or second trimester respectively, then ultrasound value was used. For unbooked patients they still have the chance to be included in our study if they can bring a scan that showed gestational age during the same period mentioned before.
  5. Idiopathic intrauterine growth restriction.
  6. Intrauterine growth restriction due to maternal malnutrition, maternal medical disorder as anemia, pregnancy induced hypertension, or chronic renal disease.
  7. Intrauterine growth restriction due to substance abuse (including smoking).
  8. With or without past history of intrauterine growth restriction .

Exclusion criteria

  1. Intrauterine growth restriction due to fetal causes as congenital abnormalities, fetal infection, or multiple gestation.
  2. Any drug therapy that can affect fetal growth or fetal blood supply.
  3. Maternal diseases that contraindicates the use of sildenafil citrate

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

54 participants in 2 patient groups

sildenafil citrate
Active Comparator group
Description:
50 mg single oral dose
Treatment:
Drug: sildenafil citrate
placebo
Active Comparator group
Description:
single tablet of placebo
Treatment:
Other: placebo

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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