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Randomized Controlled Trial Comparing a Conservative Management and Laser Surgery (TTTS1)

Primary Purpose

Blood and Blood Disorders, Anemia, Neonatal, Hematologic Disease

Status
Completed
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
Fetoscopic laser surgery
Sponsored by
Assistance Publique - Hôpitaux de Paris
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Blood and Blood Disorders focused on measuring Fetoscopic Laser surgery, Stage 1 Twin - twin transfusion syndrome

Eligibility Criteria

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

Inclusion Criteria:

  • TTTS stage 1 (Euro foetus criteria)
  • Gestational age > 16 and < 26 weeks
  • Age > 18
  • Informed consent

Exclusion Criteria:

  • Therapeutic amniocentesis prior to referral
  • Short cervix < 15 mm on transvaginal US
  • Severe maternal discomfort:Dyspnea and orthopnea, Abdominal pain > 4 on a 10-level visual analogic pain scale, Contractions > 1 per hour
  • PPROM
  • Fetal malformations unrelated to TTTS
  • Follow-up is impossible

Sites / Locations

  • Children's Hospital Colorado and Colorado Fetal Care Center
  • University of MD /Department of Obstetrics, Gynecology & Reproductive Sciences
  • Fetal Care Center of Cincinnati, Cincinnati Children's Hospital Medical Center
  • The Ohio State University / OSU Fetal Therapy Program
  • Fetal Diagnosis and Treatment, The Children's Hospital of Philadelphia
  • Fetal Treatment Program of New England, Hasbro Children's Hospital, The Warren Alpert Medical School of Brown University.
  • The Texas Fetal Center, Children's Memorial Hermann Hospital, University of Texas Medical School
  • Fetal Therapy Program, Evergrenn Hospital Medical Center
  • Mount Sinai Hospital, University of Toronto
  • Hospital Ste-Justine
  • Necker Enfants Malades

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

NO INTERVENTION

fetoscopic laser

Arm Description

Outcomes

Primary Outcome Measures

survival and neurological morbidity at the age of 6 months for each foetus randomized

Secondary Outcome Measures

Full Information

First Posted
October 11, 2010
Last Updated
July 17, 2020
Sponsor
Assistance Publique - Hôpitaux de Paris
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1. Study Identification

Unique Protocol Identification Number
NCT01220011
Brief Title
Randomized Controlled Trial Comparing a Conservative Management and Laser Surgery
Acronym
TTTS1
Official Title
A Cluster Randomized Trial Comparing a Conservative Management and Primary Laser Surgery
Study Type
Interventional

2. Study Status

Record Verification Date
July 2020
Overall Recruitment Status
Completed
Study Start Date
April 19, 2011 (Actual)
Primary Completion Date
September 30, 2018 (Actual)
Study Completion Date
March 31, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Assistance Publique - Hôpitaux de Paris

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The objective of this trial is to compare both strategies (Expectative Vs Fetoscopic laser surgery) for patients with stage 1 TTTS and favorable obstetrical parameters in an international randomized controlled trial. This trial will answer an important question and will help in the management and tailoring of surgical indications in stage 1 TTTS.
Detailed Description
Although we demonstrated the overall benefit of fetoscopic laser surgery as first-line treatment in twin-twin transfusion syndrome (TTTS), indications in early stage TTTS are controversial. Indeed, a conservative management with close follow-up is offered in some centers as first-line management for QUINTERO stage 1 TTTS, although this strategy has not been formally compared to first-line fetoscopic placental surgery. The objective of this trial is to compare both strategies for patients with stage 1 TTTS and favorable obstetrical parameters in an international randomized controlled trial. Patients randomized to a conservative management will be followed on a weekly basis as long as the syndrome remains stable using obstetrical and fetal parameters and until an adequate gestational age is reached allowing delivery. Cases progressing to stage ≥ 2 or with a worsening of obstetrical parameters during follow-up in this group will be actively treated by percutaneous laser coagulation. Patients allocated to the "immediate laser" group will be treated by fetoscopic laser surgery within 24 h following randomization. The primary end-point encompasses survival and neurological morbidity at the age of 6 months for each foetus randomized. Analyses and power computations use a cluster-trial methodology that accounts for the inter-twin correlation, with many benefits over more traditional designs using a per-pregnancy outcome. With proportions of 60% and 75% meaning a clinically relevant difference of 15% between the groups, 200 fetuses or equivalently 100 pregnancies would be needed in each arm to reach a power of 80% with an alpha-risk of 5%, allowing 2 interim analyses based upon LAN-DEMETS boundaries and an O'Brien-Fleming function. Inclusion criteria, interventions and randomisation were investigated through a preliminary survey across potential participating centers. Based on this survey, it is anticipated that 3 years will be needed to achieve the requested number of patients. This trial will answer an important question and will help in the management and tailoring of surgical indications in stage 1 TTTS.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Blood and Blood Disorders, Anemia, Neonatal, Hematologic Disease, Infant, Newborn, Diseases
Keywords
Fetoscopic Laser surgery, Stage 1 Twin - twin transfusion syndrome

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
NO INTERVENTION
Arm Type
Experimental
Arm Title
fetoscopic laser
Arm Type
Active Comparator
Intervention Type
Procedure
Intervention Name(s)
Fetoscopic laser surgery
Intervention Description
Fetoscopic laser surgery
Primary Outcome Measure Information:
Title
survival and neurological morbidity at the age of 6 months for each foetus randomized
Time Frame
6 MONTHS

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: TTTS stage 1 (Euro foetus criteria) Gestational age > 16 and < 26 weeks Age > 18 Informed consent Exclusion Criteria: Therapeutic amniocentesis prior to referral Short cervix < 15 mm on transvaginal US Severe maternal discomfort:Dyspnea and orthopnea, Abdominal pain > 4 on a 10-level visual analogic pain scale, Contractions > 1 per hour PPROM Fetal malformations unrelated to TTTS Follow-up is impossible
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Yves VILLE, PUPH
Organizational Affiliation
Assistance Publique - Hôpitaux de Paris
Official's Role
Principal Investigator
Facility Information:
Facility Name
Children's Hospital Colorado and Colorado Fetal Care Center
City
Aurora
State/Province
Colorado
ZIP/Postal Code
80045
Country
United States
Facility Name
University of MD /Department of Obstetrics, Gynecology & Reproductive Sciences
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21000
Country
United States
Facility Name
Fetal Care Center of Cincinnati, Cincinnati Children's Hospital Medical Center
City
Cincinnati
State/Province
Ohio
ZIP/Postal Code
45229-3026
Country
United States
Facility Name
The Ohio State University / OSU Fetal Therapy Program
City
Columbus
State/Province
Ohio
ZIP/Postal Code
43221
Country
United States
Facility Name
Fetal Diagnosis and Treatment, The Children's Hospital of Philadelphia
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19104
Country
United States
Facility Name
Fetal Treatment Program of New England, Hasbro Children's Hospital, The Warren Alpert Medical School of Brown University.
City
Providence
State/Province
Rhode Island
ZIP/Postal Code
02903
Country
United States
Facility Name
The Texas Fetal Center, Children's Memorial Hermann Hospital, University of Texas Medical School
City
Houston
State/Province
Texas
ZIP/Postal Code
77030
Country
United States
Facility Name
Fetal Therapy Program, Evergrenn Hospital Medical Center
City
Kirkland
State/Province
Washington
ZIP/Postal Code
98034
Country
United States
Facility Name
Mount Sinai Hospital, University of Toronto
City
Toronto
State/Province
Ontario
ZIP/Postal Code
ON M5X 1X5
Country
Canada
Facility Name
Hospital Ste-Justine
City
Montreal
State/Province
Quebec
ZIP/Postal Code
H3T 1R2
Country
Canada
Facility Name
Necker Enfants Malades
City
Paris
ZIP/Postal Code
75006
Country
France

12. IPD Sharing Statement

Citations:
PubMed Identifier
33248135
Citation
Stirnemann J, Slaghekke F, Khalek N, Winer N, Johnson A, Lewi L, Massoud M, Bussieres L, Aegerter P, Hecher K, Senat MV, Ville Y. Intrauterine fetoscopic laser surgery versus expectant management in stage 1 twin-to-twin transfusion syndrome: an international randomized trial. Am J Obstet Gynecol. 2021 May;224(5):528.e1-528.e12. doi: 10.1016/j.ajog.2020.11.031. Epub 2020 Nov 26.
Results Reference
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Randomized Controlled Trial Comparing a Conservative Management and Laser Surgery

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