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Sildenafil Citrate in Early Unexplained Recurrent Pregnancy Loss

Primary Purpose

Miscarriage, Recurrent

Status
Completed
Phase
Phase 1
Locations
Egypt
Study Type
Interventional
Intervention
Sildenafil Citrate
Folic Acid
Placebo Oral Tablet
Sponsored by
Ain Shams University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Miscarriage, Recurrent

Eligibility Criteria

20 Years - 35 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Age: 20-35 years.
  • BMI (20-30)
  • History of three or more successive unexplained recurrent miscarriage.
  • Normal uterine cavity by hystrography or hysteroscopy.
  • No luteal phase defects by progesterone > 10 ng.
  • Normal thyroid function (TSH, T3, T4)
  • Normal lupus anticoagulant measured by activated partial throbmoplastine time (32-43 seconds).
  • Normal anticardolipin (IgG < 20 gpl and IgM < 15 MPL measured by ELISA).
  • Normal anti thyroid antibodies.
  • Normal glucouse tolerance test.
  • Normal parental karyotyping.

Exclusion Criteria:

  • Age<20 or>35 year
  • BMI<20 or>30
  • Systemic diseases that might affect pregnancy such as diabetes or thyroid disorders or hypertension.
  • History of consanguinity.
  • Family history of chromosomal abnormalities (e.g. trisomy 21, trisomy 13, Turner's disease …etc.).
  • History of autoimmune diseases, eg: systemic lupus.
  • Congenital anomaly in uterine cavity as bicornate or septate uterus.
  • Luteal phase defect and corpus luteum insufficiency.
  • Uterine masses as fibroid or polyps.
  • Patient with patuoles os.
  • patient with antiphosphlipid syndrome.
  • Cigarette smoking and alcohol.

Sites / Locations

  • Ain SHams Maternity Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Sildenafil group

Control group

Arm Description

Includes 45 women who received Sildenafil citrate (Respatio(R) 25mg tablets four times daily for 24 days preconceptionally starting first day of previous period) and folic acid (Folic acid(R) 0.5mg tablets once daily for 3 months preconceptionally).

Includes 45 women who received placebo oral tablets (apparently identical to Respatio(R) 25mg tablets, four times daily for 24 days preconceptionally starting first day of previous period) and folic acid (Folic acid(R) 0.5mg tablets once daily for 3 months preconceptionally).

Outcomes

Primary Outcome Measures

Miscarriage rate
number of spontaneous/missed miscarriages among the participants in both groups

Secondary Outcome Measures

Uterine artery resistance index
Uterine artery resistance index assessed by uterine artery Doppler study in ongoing pregnancies of both groups
Uterine artery pulsatility index
Uterine artery pulsatility index assessed by uterine artery Doppler study in ongoing pregnancies of both groups

Full Information

First Posted
December 5, 2018
Last Updated
December 5, 2018
Sponsor
Ain Shams University
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1. Study Identification

Unique Protocol Identification Number
NCT03766594
Brief Title
Sildenafil Citrate in Early Unexplained Recurrent Pregnancy Loss
Official Title
Effect of Preconceptional Sildenafil Citrate Treatment in Women With Early Unexplained Recurrent Pregnancy Loss: a Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
December 2018
Overall Recruitment Status
Completed
Study Start Date
January 1, 2018 (Actual)
Primary Completion Date
November 20, 2018 (Actual)
Study Completion Date
December 1, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Ain Shams University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Recurrent unexplained spontaneous miscarriage (RSM) is defined as three consecutive pregnancy loss prior to 20 weeks from the last menstrual period. 1% to 2% of women experience RSM. Treatment of URSM is a challenging issue. The currently available lines of treatment according to simplicity of use, reliability and degree of invasiveness include corticosteroids, sildenafil citrate, aspirin, heparin and immunoglobulins (besides good antenatal care), but up to now there are no prospective randomized studies, powerful enough, to determine a significant difference between these therapeutic protocols, with any of the above mentioned pharmacological agents. Sildenafil Citrate (Viagra®), a vasodilator, is also described as an anti-inflammatory agent. While improving uterine blood flow in the proliferative phase, NO may have detrimental effects at the level of the endometrium during the implantation window. The NO- mediated release of cytokines such as tumour necrosis factor- from activated natural killer cells has been implicated as a cause of implantation failure. Based on these observations, this study attempts was made to study uterine arteries and sub-endometrial blood flow during the luteal phase in normal fertile women and in patients with Unexplained recurrent miscarriage

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Miscarriage, Recurrent

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Model Description
Patients will be randomized into two groups: Group (A) folic acid and sildenafil citrate and Group (B) folic acid and placebo. Folic acid (0.5 mg) will be started 3 months before conception in the two groups. Sildenafil citrate (dose: 25 mg; oral tablets, 4 times/day) or placebo will be started preconception for 24 days
Masking
ParticipantCare Provider
Masking Description
Patients are randomized to receive either folic acid and sildenafil citrate or folic acid and placebo. Placebo tablets were same size and appearance of the sildenafil citrate tablets.
Allocation
Randomized
Enrollment
90 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Sildenafil group
Arm Type
Active Comparator
Arm Description
Includes 45 women who received Sildenafil citrate (Respatio(R) 25mg tablets four times daily for 24 days preconceptionally starting first day of previous period) and folic acid (Folic acid(R) 0.5mg tablets once daily for 3 months preconceptionally).
Arm Title
Control group
Arm Type
Active Comparator
Arm Description
Includes 45 women who received placebo oral tablets (apparently identical to Respatio(R) 25mg tablets, four times daily for 24 days preconceptionally starting first day of previous period) and folic acid (Folic acid(R) 0.5mg tablets once daily for 3 months preconceptionally).
Intervention Type
Drug
Intervention Name(s)
Sildenafil Citrate
Intervention Description
Respatio(R) 25mg tablets four times daily for 24 days preconceptionally starting first day of previous period
Intervention Type
Drug
Intervention Name(s)
Folic Acid
Intervention Description
Folic acid(R) 0.5mg tablets once daily for 3 months preconceptionally
Intervention Type
Drug
Intervention Name(s)
Placebo Oral Tablet
Intervention Description
Placebo tablet apparently identical to Respatio(R) 25mg tablets, taken four times daily for 24 days preconceptionally starting first day of previous period
Primary Outcome Measure Information:
Title
Miscarriage rate
Description
number of spontaneous/missed miscarriages among the participants in both groups
Time Frame
24 gestational weeks
Secondary Outcome Measure Information:
Title
Uterine artery resistance index
Description
Uterine artery resistance index assessed by uterine artery Doppler study in ongoing pregnancies of both groups
Time Frame
At 24 gestational weeks
Title
Uterine artery pulsatility index
Description
Uterine artery pulsatility index assessed by uterine artery Doppler study in ongoing pregnancies of both groups
Time Frame
At 24 gestational weeks

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
35 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age: 20-35 years. BMI (20-30) History of three or more successive unexplained recurrent miscarriage. Normal uterine cavity by hystrography or hysteroscopy. No luteal phase defects by progesterone > 10 ng. Normal thyroid function (TSH, T3, T4) Normal lupus anticoagulant measured by activated partial throbmoplastine time (32-43 seconds). Normal anticardolipin (IgG < 20 gpl and IgM < 15 MPL measured by ELISA). Normal anti thyroid antibodies. Normal glucouse tolerance test. Normal parental karyotyping. Exclusion Criteria: Age<20 or>35 year BMI<20 or>30 Systemic diseases that might affect pregnancy such as diabetes or thyroid disorders or hypertension. History of consanguinity. Family history of chromosomal abnormalities (e.g. trisomy 21, trisomy 13, Turner's disease …etc.). History of autoimmune diseases, eg: systemic lupus. Congenital anomaly in uterine cavity as bicornate or septate uterus. Luteal phase defect and corpus luteum insufficiency. Uterine masses as fibroid or polyps. Patient with patuoles os. patient with antiphosphlipid syndrome. Cigarette smoking and alcohol.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mohamed Yakout, MBBCh
Organizational Affiliation
M Yakout
Official's Role
Principal Investigator
Facility Information:
Facility Name
Ain SHams Maternity Hospital
City
Cairo
State/Province
Abbaseya
ZIP/Postal Code
002
Country
Egypt

12. IPD Sharing Statement

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