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Pessary to Prevent Prematurity in Twins in Case of Short Cervix (PESSAR'ONE)

Primary Purpose

Pregnancy

Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Pessary
Sponsored by
University Hospital, Toulouse
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Pregnancy focused on measuring prematurity, short cervix, twin pregnancy, pessary

Eligibility Criteria

18 Years - 60 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

Asymptomatic twin pregnancies between 16 and 24+0 weeks CL < 25th percentile for GA

- < 35mm between 16 and 24+0d weeks Vaginal swabs for bacteriological analysis < 72 hours Patient age > 18 years Written informed consent obtained French first language (speak, read, understand) French social security cover

Exclusion Criteria:

  • Painful regular contractions
  • Major fetal abnormalities
  • Fetal malformation
  • Active vaginal bleeding, placenta praevia
  • Discordance fetal weight more than 40%
  • Treatment with progesterone
  • Patient with cerclage
  • Ruptured of membrane
  • Twin to twin transfusion syndrome
  • Uterine malformation
  • Chronic maternal disease (diabetes, hypertension, renal insufficiency, Heparin Treatment)
  • Conisation history
  • patients subject to a judicial safeguard order, participating in another research study including an exclusion period which has not expired at the time of screening will not be included

Sites / Locations

  • CHU Angers
  • CHU Bordeaux
  • CHU Caen
  • CHRU Lille
  • Hôpital Marseille AP-HM
  • Hôpital Saint-Joseph
  • CHU Nantes
  • GH Pitié Salpétriêre
  • Hôpital Antoine Béclère
  • Hôpital Bicêtre
  • Hôpital Necker
  • Hôpital Robert Debré
  • Maternité Port-Royal Cochin
  • CHI Poissy
  • CHU Saint-Etienne
  • Hôpital Universitaire de Strasbourg
  • CHU Toulouse
  • CHU Tours

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Pessary

No pessary

Arm Description

The device will be placed in the vagina during the consultation. It is rinsed in sterile water for lubrification and left in place until delivery or remove at 36 weeks in case of no delivery before. There is no need to use any analgesia. The good position of the pessary is checking in the same time than the placement with digital examination.

No pessary will be placed in the vagina.

Outcomes

Primary Outcome Measures

perinatal death or significant neonatal morbidity until discharge from the hospital
it's a composite outcome : perinatal death (i.e medical interruption of pregnancy, intrauterine fetal death, or death occurring during the first four weeks after birth, before day 29), or significant neonatal morbidity until discharge from the hospital, defined as one or more of the following complications: bronchopulmonary dysplasia (BPD), intraventricular haemorrhage (IVH) grade III or IV, periventricular leucomalacia (PVL), necrotizing enterocolitis (NEC) grade II or higher, culture proven sepsis, retinopathy of prematurity (ROP) requiring treatment.

Secondary Outcome Measures

Preterm delivery
To evaluate the prolongation of pregnancy in days
The differential cost-efficacy ratio of the two strategies
Tolerance of the pessary

Full Information

First Posted
October 1, 2014
Last Updated
July 28, 2020
Sponsor
University Hospital, Toulouse
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1. Study Identification

Unique Protocol Identification Number
NCT02328989
Brief Title
Pessary to Prevent Prematurity in Twins in Case of Short Cervix
Acronym
PESSAR'ONE
Official Title
Pessary to Prevent Prematurity in Twins in Case of Short Cervix
Study Type
Interventional

2. Study Status

Record Verification Date
July 2020
Overall Recruitment Status
Completed
Study Start Date
November 2014 (undefined)
Primary Completion Date
October 2018 (Actual)
Study Completion Date
October 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Toulouse

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
For 25 years, the twin pregnancy rate has regularly increased in the majority of European countries and in the United States, by 35% between 1981 and 2006. Increased use of medically assisted procreation and older maternal age are the two main causes. At the present time twin pregnancies represent nearly 20% of premature deliveries. The rate of very premature births (< 32-34 weeks) is 7 times higher in twin pregnancies than in singleton pregnancies. As prematurity accounts for 75% of neonatal morbidity and mortality, and extreme prematurity is the principal cause of neonatal mortality and of brain sequelae in twins, the search for a preventive treatment appears as a priority in perinatal medicine. The investigators recently showed in a prospective multicenter study that cervical ultrasound at 22 and 27 wks was a better predictive investigation of premature delivery < 34 wks than digital examination. Recently in a randomized trial in a population of short-cervix singleton pregnancies, the premature delivery rate decreased by 40% in the pessary group compared with the usual management group. No other trial of pessary use in short-cervix twin pregnancies was published today. Recently, in a historical comparison of twins with twin-to-twin transfusion syndrome treated with laser, Carreras et al. have showed a decreased rate of preterm delivery with the use of pessary in case of short cervix. The investigators wish to set up a randomized multicenter study in France in the population of short-cervix twin pregnancies to show a potential benefit of the pessary compared with simple surveillance.
Detailed Description
For 25 years, the twin pregnancy rate has regularly increased in the majority of European countries and in the United States, by 35% between 1981 and 2006. Increased use of medically assisted procreation and older maternal age are the two main causes. At the present time twin pregnancies represent nearly 20% of premature deliveries. The rate of very premature births (< 32-34 weeks) is 7 times higher in twin pregnancies than in singleton pregnancies. As prematurity accounts for 75% of neonatal morbidity and mortality, and extreme prematurity is the principal cause of neonatal mortality and of brain sequelae in twins, the search for a preventive treatment appears as a priority in perinatal medicine. The investigators recently showed in a prospective multicenter study that cervical ultrasound at 22 and 27 wks was a better predictive investigation of premature delivery < 34 wks than digital examination.[1] As there is currently no recommended preventive treatment for prematurity in twin pregnancies[2], the 2009 guidelines of the College of Obstetricians leave the teams with the option of carrying out systematic cervical ultrasound or not during follow-up investigations.[3] Recently in a randomized trial in a population of short-cervix singleton pregnancies, the premature delivery rate decreased by 40% in the pessary group compared with the usual management group.[4] In a recent multicenter trial (ProTWIN), while therapeutic efficacy of the pessary (versus usual management) was not demonstrated in the overall group of twin pregnancies, in the short-cervix subgroup (< 25th percentile of the population) the < 32 wks delivery rate decreased from 29% to 14% (OR= 0.49 (0.24-0.97) and neonatal morbidity also decreased.[5] No other trial of pessary use in short-cervix twin pregnancies was published today. Recently, in a historical comparison of twins with twin-to-twin transfusion syndrome treated with laser, Carreras et al. have showed a decreased rate of preterm delivery with the use of pessary in case of short cervix.[6] The investigators wish to set up a randomized multicenter study in France in the population of short-cervix twin pregnancies to show a potential benefit of the pessary compared with simple surveillance.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pregnancy
Keywords
prematurity, short cervix, twin pregnancy, pessary

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
324 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Pessary
Arm Type
Experimental
Arm Description
The device will be placed in the vagina during the consultation. It is rinsed in sterile water for lubrification and left in place until delivery or remove at 36 weeks in case of no delivery before. There is no need to use any analgesia. The good position of the pessary is checking in the same time than the placement with digital examination.
Arm Title
No pessary
Arm Type
No Intervention
Arm Description
No pessary will be placed in the vagina.
Intervention Type
Device
Intervention Name(s)
Pessary
Intervention Description
The device will be placed in the vagina during the consultation. It is rinsed in sterile water for lubrification and left in place until delivery or remove at 36 weeks in case of no delivery before. There is no need to use any analgesia. The good position of the pessary is checking in the same time than the placement with digital examination.
Primary Outcome Measure Information:
Title
perinatal death or significant neonatal morbidity until discharge from the hospital
Description
it's a composite outcome : perinatal death (i.e medical interruption of pregnancy, intrauterine fetal death, or death occurring during the first four weeks after birth, before day 29), or significant neonatal morbidity until discharge from the hospital, defined as one or more of the following complications: bronchopulmonary dysplasia (BPD), intraventricular haemorrhage (IVH) grade III or IV, periventricular leucomalacia (PVL), necrotizing enterocolitis (NEC) grade II or higher, culture proven sepsis, retinopathy of prematurity (ROP) requiring treatment.
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Preterm delivery
Time Frame
6 months
Title
To evaluate the prolongation of pregnancy in days
Time Frame
6 months
Title
The differential cost-efficacy ratio of the two strategies
Time Frame
6 months
Title
Tolerance of the pessary
Time Frame
6 months

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Asymptomatic twin pregnancies between 16 and 24+0 weeks CL < 25th percentile for GA - < 35mm between 16 and 24+0d weeks Vaginal swabs for bacteriological analysis < 72 hours Patient age > 18 years Written informed consent obtained French first language (speak, read, understand) French social security cover Exclusion Criteria: Painful regular contractions Major fetal abnormalities Fetal malformation Active vaginal bleeding, placenta praevia Discordance fetal weight more than 40% Treatment with progesterone Patient with cerclage Ruptured of membrane Twin to twin transfusion syndrome Uterine malformation Chronic maternal disease (diabetes, hypertension, renal insufficiency, Heparin Treatment) Conisation history patients subject to a judicial safeguard order, participating in another research study including an exclusion period which has not expired at the time of screening will not be included
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Christophe Vayssière, PhD
Organizational Affiliation
CHU Toulouse
Official's Role
Study Director
Facility Information:
Facility Name
CHU Angers
City
Angers
Country
France
Facility Name
CHU Bordeaux
City
Bordeaux
Country
France
Facility Name
CHU Caen
City
Caen
Country
France
Facility Name
CHRU Lille
City
Lille
Country
France
Facility Name
Hôpital Marseille AP-HM
City
Marseille
Country
France
Facility Name
Hôpital Saint-Joseph
City
Marseille
Country
France
Facility Name
CHU Nantes
City
Nantes
Country
France
Facility Name
GH Pitié Salpétriêre
City
Paris
Country
France
Facility Name
Hôpital Antoine Béclère
City
Paris
Country
France
Facility Name
Hôpital Bicêtre
City
Paris
Country
France
Facility Name
Hôpital Necker
City
Paris
Country
France
Facility Name
Hôpital Robert Debré
City
Paris
Country
France
Facility Name
Maternité Port-Royal Cochin
City
Paris
Country
France
Facility Name
CHI Poissy
City
Poissy
Country
France
Facility Name
CHU Saint-Etienne
City
Saint-Etienne
Country
France
Facility Name
Hôpital Universitaire de Strasbourg
City
Strasbourg
Country
France
Facility Name
CHU Toulouse
City
Toulouse
ZIP/Postal Code
31059
Country
France
Facility Name
CHU Tours
City
Tours
Country
France

12. IPD Sharing Statement

Plan to Share IPD
No

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Pessary to Prevent Prematurity in Twins in Case of Short Cervix

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