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The Trial of Pessary After Laser for TTTS (PECEPLASER)

Primary Purpose

Premature Birth

Status
Terminated
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
Arabin Cervical Pessary
Sponsored by
Hospital Universitari Vall d'Hebron Research Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Premature Birth focused on measuring Monochorionic pregnancy, Twin to twin transfusion syndrome, Cervical pessary, Cervical length

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Monochorionic twin pregnancies with severe TTTS requiring intrauterine surgery
  • Less than 26 weeks
  • Minimal age of 18 years
  • Informed consent signature

Exclusion Criteria:

  • Major fetal abnormalities (requiring surgery or leading to infant death or severe handicap)
  • Cerclage prior to randomisation
  • Uterine malformation
  • Placenta previa
  • Active vaginal bleeding at the moment of randomization
  • Spontaneous rupture of membranes at the time of randomization
  • Death of both twins after the surgery
  • Monochorionic-monoamniotic twin pregnancy
  • Silicone allergy
  • Current participation in other RCT

Sites / Locations

  • UZ Leuven. Campus Gasthuisberg
  • Frauenklinik - Zentrum für Ultraschalldiagnostik und Pränatalmedizin Bürgerhospital und Clementine Kinderhospital gemeinnützige GmbH
  • University Medical Center Eppendorf
  • Hospital Universitari Vall d'Hebron

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Other

Arm Label

Usual management

Arabin Cervical Pessary

Arm Description

Usual management of monochorionic pregnancy without the pessary placement

The pessary will be inserted 24 hours after fetal surgery in the exploration room. This procedure does not need anaesthesia and it does not need to be done in a surgery room. During the following explorations the correct placement of the pessary is assessed, and if it does not, it can be easily adjusted. The pessary will be removed at 37 weeks of gestation, or before if any unexpected event occurs.

Outcomes

Primary Outcome Measures

Delivery before 32 weeks
Rate of delivery before 32 weeks

Secondary Outcome Measures

Birth weight
Median weight (g) of the newborns at birth.
Fetal or neonatal death
Rate of intrauterine demise or neonatal death during the first 24 hours.
Neonatal morbidity
Rate of major adverse neonatal outcomes before discharge from the hospital.
Significant maternal adverse events
Rate of heavy bleeding (bleeding that requires a medical intervention), cervical tear (cervical rupture due to the pessary placement), and/or uterine rupture (rupture of the uterus due to contractions or surgery).
Physical or psychological intolerance to pessary
Discomfort or pain due to the pessary that makes daily life uncomfortable (number of cases).
Preterm birth before 37 weeks
Rate of delivery before 36+6 weeks
Rupture of membranes before 32 weeks
Rupture of amniotic membranes before 31+6 weeks
Hospitalisation for threatened preterm labour before 32 weeks
Requirement of hospitalisation due to preterm contractions that need medical treatment to try to stop them before 31+6 weeks (rate).
Time to birth
Preterm birth before 34 weeks
rate of delivery before 33+6 weeks
Preterm birth before 30 weeks
rate of delivery before 29+6 weeks
Preterm birth before 28 weeks
rate of delivery before 27+6 weeks

Full Information

First Posted
April 12, 2011
Last Updated
August 25, 2020
Sponsor
Hospital Universitari Vall d'Hebron Research Institute
Collaborators
Maternal-Infantil Vall d´Hebron Hospital, Universitaire Ziekenhuizen KU Leuven, Universitätsklinikum Hamburg-Eppendorf, Bürgerhospital Frankfurt
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1. Study Identification

Unique Protocol Identification Number
NCT01334489
Brief Title
The Trial of Pessary After Laser for TTTS
Acronym
PECEPLASER
Official Title
Arabin Cervical Pessary for Prevention of Preterm Birth in Cases of Twin-to-twin Transfusion Syndrome Treated by Fetoscopic Laser Coagulation: The PECEP Laser Trial
Study Type
Interventional

2. Study Status

Record Verification Date
August 2020
Overall Recruitment Status
Terminated
Why Stopped
Interim analysis unfavorable to continue the study
Study Start Date
December 2012 (Actual)
Primary Completion Date
January 2020 (Actual)
Study Completion Date
June 25, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Hospital Universitari Vall d'Hebron Research Institute
Collaborators
Maternal-Infantil Vall d´Hebron Hospital, Universitaire Ziekenhuizen KU Leuven, Universitätsklinikum Hamburg-Eppendorf, Bürgerhospital Frankfurt

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Placing a cervical pessary in severe twin-to-twin transfusion syndrome (TTTS) cases treated by fetoscopic laser coagulation (FLC) decreases the spontaneous preterm birth rate.
Detailed Description
Monochorionic (MC) twin pregnancies present with a high rate of fetal complications, most of them associated with the placental vascular anastomoses. Fetoscopic laser coagulation (FLC) is a surgical technique that allows minimally invasive access into the uterus and has emerged as a useful tool in the management of the most common and severe of these complications, twin to twin transfusion syndrome (TTTS). Even though, preterm birth remains a common cause of adverse outcome because TTTS is associated with a 29% risk of delivering before 28 weeks. A short cervical length (CL), defined as a CL ≤ 25 mm, detected by transvaginal ultrasound is an independent risk factor for preterm birth in twin pregnancies but no effective treatment has been described to prevent it. Although is usually accepted that in twin pregnancies cerclage may increase the risk of preterm birth, Salomon and co-workers, found that in cases of TTTS with a CL below the 5th percentile (15 mm) at the time of surgery, performing an emergency cerclage prolonged the pregnancy and allow for better outcome, But still preterm birth after FLC remains a big challenge, so new methods to prevent it must be investigated. Previous studies in singletons and twins have shown that the use of cervical pessary significantly reduces the frequency of birth before 32 weeks and prolongs pregnancy. The advantage of using cervical pessary is that it is less invasive than cerclage and can be removed easily. That's the reason why pessaries could be considered an alternative, non invasive option to prevent preterm birth in cases of twin to twin transfusion syndrome (TTTS) treated by laser surgery.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Premature Birth
Keywords
Monochorionic pregnancy, Twin to twin transfusion syndrome, Cervical pessary, Cervical length

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
352 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Usual management
Arm Type
No Intervention
Arm Description
Usual management of monochorionic pregnancy without the pessary placement
Arm Title
Arabin Cervical Pessary
Arm Type
Other
Arm Description
The pessary will be inserted 24 hours after fetal surgery in the exploration room. This procedure does not need anaesthesia and it does not need to be done in a surgery room. During the following explorations the correct placement of the pessary is assessed, and if it does not, it can be easily adjusted. The pessary will be removed at 37 weeks of gestation, or before if any unexpected event occurs.
Intervention Type
Device
Intervention Name(s)
Arabin Cervical Pessary
Intervention Description
The Arabin cervical pessary, which is CE-certified for preventing SPB (CE 0482 / EN ISO 13485: 2003 annex III of the council directive 93/42 EEC). It is a vaginal device which is used to treat pregnant women for preventing spontaneous preterm birth. This device can be easily placed around the uterine cervix without pain.
Primary Outcome Measure Information:
Title
Delivery before 32 weeks
Description
Rate of delivery before 32 weeks
Time Frame
Within the first 15 days after delivery
Secondary Outcome Measure Information:
Title
Birth weight
Description
Median weight (g) of the newborns at birth.
Time Frame
Within the first 15 days after delivery
Title
Fetal or neonatal death
Description
Rate of intrauterine demise or neonatal death during the first 24 hours.
Time Frame
Within the first 15 days after the death
Title
Neonatal morbidity
Description
Rate of major adverse neonatal outcomes before discharge from the hospital.
Time Frame
30 days after the discharge from the hospital
Title
Significant maternal adverse events
Description
Rate of heavy bleeding (bleeding that requires a medical intervention), cervical tear (cervical rupture due to the pessary placement), and/or uterine rupture (rupture of the uterus due to contractions or surgery).
Time Frame
Within 15 days after discharge from the hospital
Title
Physical or psychological intolerance to pessary
Description
Discomfort or pain due to the pessary that makes daily life uncomfortable (number of cases).
Time Frame
Within 15 days after discharge from hospital
Title
Preterm birth before 37 weeks
Description
Rate of delivery before 36+6 weeks
Time Frame
Within 15 days after delivery
Title
Rupture of membranes before 32 weeks
Description
Rupture of amniotic membranes before 31+6 weeks
Time Frame
Within 15 days after delivery
Title
Hospitalisation for threatened preterm labour before 32 weeks
Description
Requirement of hospitalisation due to preterm contractions that need medical treatment to try to stop them before 31+6 weeks (rate).
Time Frame
Within 15 days after delivery
Title
Time to birth
Time Frame
Within 15 days after delivery
Title
Preterm birth before 34 weeks
Description
rate of delivery before 33+6 weeks
Time Frame
Within 15 days after delivery
Title
Preterm birth before 30 weeks
Description
rate of delivery before 29+6 weeks
Time Frame
Within 15 days after delivery
Title
Preterm birth before 28 weeks
Description
rate of delivery before 27+6 weeks
Time Frame
Within 15 days after delivery

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Monochorionic twin pregnancies with severe TTTS requiring intrauterine surgery Less than 26 weeks Minimal age of 18 years Informed consent signature Exclusion Criteria: Major fetal abnormalities (requiring surgery or leading to infant death or severe handicap) Cerclage prior to randomisation Uterine malformation Placenta previa Active vaginal bleeding at the moment of randomization Spontaneous rupture of membranes at the time of randomization Death of both twins after the surgery Monochorionic-monoamniotic twin pregnancy Silicone allergy Current participation in other RCT
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Elena Carreras, PhD
Organizational Affiliation
Hospital Vall d'Hebron
Official's Role
Principal Investigator
Facility Information:
Facility Name
UZ Leuven. Campus Gasthuisberg
City
Leuven
ZIP/Postal Code
3000
Country
Belgium
Facility Name
Frauenklinik - Zentrum für Ultraschalldiagnostik und Pränatalmedizin Bürgerhospital und Clementine Kinderhospital gemeinnützige GmbH
City
Frankfurt
ZIP/Postal Code
60318
Country
Germany
Facility Name
University Medical Center Eppendorf
City
Hamburg
ZIP/Postal Code
20246
Country
Germany
Facility Name
Hospital Universitari Vall d'Hebron
City
Barcelona
ZIP/Postal Code
08035
Country
Spain

12. IPD Sharing Statement

Citations:
PubMed Identifier
23055333
Citation
Carreras E, Arevalo S, Bello-Munoz JC, Goya M, Rodo C, Sanchez-Duran MA, Peiro JL, Cabero L. Arabin cervical pessary to prevent preterm birth in severe twin-to-twin transfusion syndrome treated by laser surgery. Prenat Diagn. 2012 Dec;32(12):1181-5. doi: 10.1002/pd.3982. Epub 2012 Oct 11.
Results Reference
background
PubMed Identifier
22475493
Citation
Goya M, Pratcorona L, Merced C, Rodo C, Valle L, Romero A, Juan M, Rodriguez A, Munoz B, Santacruz B, Bello-Munoz JC, Llurba E, Higueras T, Cabero L, Carreras E; Pesario Cervical para Evitar Prematuridad (PECEP) Trial Group. Cervical pessary in pregnant women with a short cervix (PECEP): an open-label randomised controlled trial. Lancet. 2012 May 12;379(9828):1800-6. doi: 10.1016/S0140-6736(12)60030-0. Epub 2012 Apr 3. Erratum In: Lancet. 2012 May 12;379(9828):1790.
Results Reference
background
PubMed Identifier
21305638
Citation
Goya M, Pratcorona L, Higueras T, Perez-Hoyos S, Carreras E, Cabero L. Sonographic cervical length measurement in pregnant women with a cervical pessary. Ultrasound Obstet Gynecol. 2011 Aug;38(2):205-9. doi: 10.1002/uog.8960. Epub 2011 Jul 18.
Results Reference
background
PubMed Identifier
23924878
Citation
Liem S, Schuit E, Hegeman M, Bais J, de Boer K, Bloemenkamp K, Brons J, Duvekot H, Bijvank BN, Franssen M, Gaugler I, de Graaf I, Oudijk M, Papatsonis D, Pernet P, Porath M, Scheepers L, Sikkema M, Sporken J, Visser H, van Wijngaarden W, Woiski M, van Pampus M, Mol BW, Bekedam D. Cervical pessaries for prevention of preterm birth in women with a multiple pregnancy (ProTWIN): a multicentre, open-label randomised controlled trial. Lancet. 2013 Oct 19;382(9901):1341-9. doi: 10.1016/S0140-6736(13)61408-7. Epub 2013 Aug 5.
Results Reference
background
PubMed Identifier
28764674
Citation
Rodo C, Arevalo S, Lewi L, Couck I, Hollwitz B, Hecher K, Carreras E. Arabin cervical pessary for prevention of preterm birth in cases of twin-to-twin transfusion syndrome treated by fetoscopic LASER coagulation: the PECEP LASER randomised controlled trial. BMC Pregnancy Childbirth. 2017 Aug 1;17(1):256. doi: 10.1186/s12884-017-1435-0.
Results Reference
derived
Links:
URL
https://dr-arabin.de/product-category/products/obstetrics/?lang=en
Description
Arabin Cervical Pessary

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The Trial of Pessary After Laser for TTTS

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