Suspended

Vaginal Progesterone to Prevent Early Preterm Birth In Twin Pregnancy With Short Cervix. Double-Blind, Placebo-Controlled, Randomized Clinical Trial

0 criteria met from your profileSee at a glance how your profile meets each eligibility criteria.
What is being tested

Vaginal Progesterone gel.

+ fetal fibronectin swab.

+ fetal fibronectin swab.

DrugProcedure
Who is being recruted

Urogenital Diseases+3

+ Female Urogenital Diseases and Pregnancy Complications

+ Obstetric Labor Complications

From 18 to 60 Years
See all eligibility criteria
How is the trial designed

Treatment Study

Placebo-ControlledPhase 2 & 3
Interventional
Study Start: March 2014
See protocol details

Summary

Principal SponsorObstetrix Medical Group
Last updated: December 19, 2014
Sourced from a government-validated database.Claim as a partner

Study start date: March 1, 2014

Actual date on which the first participant was enrolled.

This is a placebo-controlled, double-blind, randomized clinical trial of asymptomatic women with twin pregnancy and a cervix length 10 mm to 25 mm discovered on a routine screening transvaginal sonogram between 20w0d to 24w0d gestational age. Women will be randomized in either the in-patient or out-patient setting (1:1) to a daily vaginal application of micronized progesterone cream(200 mg)vs. placebo to determine if daily vaginal progesterone administration reduces the risk of preterm birth prior to 34w0d of gestation.

Principal SponsorObstetrix Medical Group
Last updated: December 19, 2014
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.

Treatment Study

These studies test new ways to treat a disease, condition, or health issue. The goal is to see if a new drug, therapy, or approach works better or has fewer side effects than existing options.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Female

Biological sex of participants that are eligible to enroll.

From 18 to 60 Years

Range of ages for which participants are eligible to join.

Healthy volunteers allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Urogenital DiseasesFemale Urogenital Diseases and Pregnancy ComplicationsObstetric Labor ComplicationsObstetric Labor, PrematurePregnancy ComplicationsPremature Birth

Criteria

Inclusion Criteria: Gestational age between 20w0d and 24w0d Twin pregnancy, diamniotic-dichorionic, both twins living Cervical length 10 mm to 25 mm discovered by a screening transvaginal ultrasound exam Exclusion Criteria: Mother less than 18 years of age Uterine contractions of 40 seconds duration or more, 10 or more per hour Rupture of fetal membranes (leakage of amniotic fluid one or both sacs) Ongoing vaginal bleeding Any condition likely to cause serious neonatal morbidity independent of gestational age, including: fetal malformation likely to require surgery fetal malformation involving vital organs fetal viral infection hydrops fetalis discordance in estimated fetal weight more than 10% velamentous insertion of umbilical cord of either twin placenta previa of either placenta Any contraindication to continuing the pregnancy Cervical cerclage in place or planned Any contraindication to vaginal micronized progesterone, including: Known sensitivity to progesterone or any of the other ingredients Liver dysfunction or disease Known or suspected malignancy of breast or genital organs Active thromboembolic disorder, or history of hormone-associated thromboembolic disorder

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

2 intervention groups are designated in this study

50% chance of being blinded to the placebo group

Treatment Groups

Group I

Active Comparator
Daily administration of Vaginal Progesterone (200mg) Gel between 20 weeks of pregnancy and 34 weeks of pregnancy.

Group II

Placebo
Daily vaginal administration of Placebo gel (Vanicream)between 20 weeks of pregnancy and 34 weeks of pregnancy.

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Good Samaritan Hospital

San Jose, United StatesOpen Good Samaritan Hospital in Google Maps
SuspendedOne Study Center