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Comparison Between Natural Progesterone and Vaginal Pessary for the Prevention of Spontaneous Preterm Birth (PROPE)

Primary Purpose

Preterm Labor, Premature Birth

Status
Unknown status
Phase
Phase 4
Locations
Brazil
Study Type
Interventional
Intervention
natural progesterone
cervical pessary
Sponsored by
University of Sao Paulo
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Preterm Labor focused on measuring progesterone, uterine cervix, cervical pessary

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • gestational age between 20 weeks and 23 weeks and 6 days
  • singleton pregnancies

Exclusion Criteria:

  • no confirmation of the gestational age
  • ruptured membranes
  • painful regular uterine contractions
  • major fetal abnormalities

Sites / Locations

  • Hospital das Clínicas da Faculdade de Medicina da USPRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

cervical pessary

natural progesterone

Arm Description

Patients with uterine cervical length ≤ 25 mm are randomized to use the cervical pessary or natural progesterone to compare their effectiveness in the reduction of preterm birth rates.

Patients with uterine cervical length ≤ 25 mm are randomized to use the cervical pessary or natural progesterone to compare their effectiveness in the reduction of preterm birth rates.

Outcomes

Primary Outcome Measures

Preterm birth rate before 34 complete weeks of gestation

Secondary Outcome Measures

Full Information

First Posted
July 6, 2015
Last Updated
July 31, 2018
Sponsor
University of Sao Paulo
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1. Study Identification

Unique Protocol Identification Number
NCT02511574
Brief Title
Comparison Between Natural Progesterone and Vaginal Pessary for the Prevention of Spontaneous Preterm Birth
Acronym
PROPE
Official Title
Comparison Between Natural Progesterone and Vaginal Pessary for the Prevention of Spontaneous Preterm Birth in Pregnant Women With a Uterine Cervix Measuring 25 mm or Less in Length
Study Type
Interventional

2. Study Status

Record Verification Date
July 2018
Overall Recruitment Status
Unknown status
Study Start Date
June 2014 (Actual)
Primary Completion Date
December 2019 (Anticipated)
Study Completion Date
December 2020 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Sao Paulo

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The aim of this study is to compare the effectiveness between the cervical pessary and the natural progesterone in reduction of preterm birth rates in pregnant women with a uterine cervical length of 25 mm or less evaluated by transvaginal ultrasonography.
Detailed Description
Preterm birth is the leading cause of perinatal morbidity and mortality. The rates of spontaneous premature labor have not changed much during the past 10 years. A significant decrease in mortality and morbidity of premature babies will only be possible if women at risk of spontaneous preterm birth are accurately identified and administered preventive therapies. Ultrasonographic measurement of the cervix between 20 and 24 weeks of gestation can improve the identification of both women with single pregnancies and those with twin pregnancies at risk. Asymptomatic women with a short uterine cervix (25 mm or less) are at increased risk of spontaneous premature labor. The prophylactic use of progesterone during the early phase of pregnancy in women with a history of preterm birth and those with a short cervix can prevent preterm birth. The cervical pessary is a device used also for the prevention of preterm birth. The omega-3 intake also appears to be related to the prevention of prematurity. Vaginal infections are also important causes of preterm birth. There are not many studies about the vaginal microbiome in pregnant women. Measurement of cervical length is used as a screening test because it is inexpensive, has a short learning curve, and is well tolerated by patients. In addition, placement and removal of the pessary is an easy, accessible, and noninvasive procedure. The results on the concentration of omega 3 and preterm birth are still conflicting. The aim of this study is to compare the effectiveness of the cervical pessary and the natural progesterone in reduction of preterm birth rates in pregnant women with a uterine cervix measuring 25 mm or less in length as evaluated by transvaginal ultrasonography, assess whether there is a relationship between maternal plasma concentration of omega 3 and preterm birth, and compare the microbiome in these women. Methods: A prospective randomized controlled trial including pregnant women at the time of morphological ultrasound between 20 and 23 weeks and 6 days of pregnancy. Pregnant women in this gestational age with cervical length of 25 mm or less will be randomized between the conduct and the inclusion of progesterone vaginal pessary. In patients of both groups vaginal discharge sample will be collected at the time of randomization. In all pregnant women who accept participate in the study (short cervix or not) will be collected blood sample for measurement of omega 3.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Preterm Labor, Premature Birth
Keywords
progesterone, uterine cervix, cervical pessary

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
200 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
cervical pessary
Arm Type
Experimental
Arm Description
Patients with uterine cervical length ≤ 25 mm are randomized to use the cervical pessary or natural progesterone to compare their effectiveness in the reduction of preterm birth rates.
Arm Title
natural progesterone
Arm Type
Active Comparator
Arm Description
Patients with uterine cervical length ≤ 25 mm are randomized to use the cervical pessary or natural progesterone to compare their effectiveness in the reduction of preterm birth rates.
Intervention Type
Drug
Intervention Name(s)
natural progesterone
Intervention Type
Device
Intervention Name(s)
cervical pessary
Primary Outcome Measure Information:
Title
Preterm birth rate before 34 complete weeks of gestation
Time Frame
before 34 weeks of gestation

10. Eligibility

Sex
Female
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: gestational age between 20 weeks and 23 weeks and 6 days singleton pregnancies Exclusion Criteria: no confirmation of the gestational age ruptured membranes painful regular uterine contractions major fetal abnormalities
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Mario Henrique B Carvalho
Phone
+55 11 26616380
Email
marioburlacchini@uol.com.br
First Name & Middle Initial & Last Name or Official Title & Degree
Juliana VC Marinelli
Phone
+55 11 996911245
Email
jucodato@gmail.com
Facility Information:
Facility Name
Hospital das Clínicas da Faculdade de Medicina da USP
City
São Paulo
ZIP/Postal Code
05403-000
Country
Brazil
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Mario Henrique B Carvalho
Phone
+55 11 2661-6380
Email
marioburlacchini@uol.com.br

12. IPD Sharing Statement

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Comparison Between Natural Progesterone and Vaginal Pessary for the Prevention of Spontaneous Preterm Birth

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