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A PROSPECTIVE STUDY ON THE ROLE OF KARL STORZ CURVED AND STRAIGHT FETOSCOPES (11508AAK and 11506AAK) FOR FETOSCOPIC INTRAUTERINE PROCEDURES

Primary Purpose

Fetal Conditions, Maternal; Procedure, Pregnancy Related

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Karl Storz Curved (11508AAK) and Straight (11506AAK) Fetoscopes
Sponsored by
Boston Children's Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Fetal Conditions focused on measuring Fetoscope, Fetoscopic Laser Ablation, Diagnostic Fetoscopy

Eligibility Criteria

18 Years - 45 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria: Pregnant patient with a condition requiring in-utero surgery Patient must be eligible for anesthesia Patient and father of the fetus (if available) are able to provide signed informed consent Exclusion Criteria: Allergy or previous adverse reaction to any ancillary medication specified in this protocol that has no alternative Preterm labor, preeclampsia, or uterine anomaly (e.g., large fibroid tumor) in the index pregnancy Suspicion of major recognized congenital syndrome on ultrasound or MRI that is not compatible with postnatal life Pre-pregnancy maternal BMI greater than 40 High risk for fetal hemophilia Fetal aneuploidy or variants of known significance if an amniocentesis was performed Contraindication to abdominal surgery or fetoscopic surgery

Sites / Locations

    Arms of the Study

    Arm 1

    Arm Type

    Experimental

    Arm Label

    Karl Storz Curved or Straight Scope

    Arm Description

    A Karl Storz Curved (11508AAK) or Straight (11506AAK) Fetoscope will be used to provide visualization during in-utero (in the womb) diagnostic and interventional procedures. The curved scope will be used in patients with a placenta that sits at the front of their uterus. The straight scope will be used in patients with a placenta that sits at the back of their uterus.

    Outcomes

    Primary Outcome Measures

    Rate of completed fetoscopic procedures
    The rate of successfully completed intrauterine procedures (out of 50 total) using the Karl Storz Curved (11508AAK) or Straight (11506AAk) Fetoscope will be measured.
    Fetal survival at birth
    The number of fetuses who undergo an intrauterine fetoscopic procedure using these devices and survive at birth will be analyzed.

    Secondary Outcome Measures

    Successful visualization of all targeted vessels
    The rate of procedures with these fetoscopes in which there is successful visualization of the targeted vessels will be studied. This measure will be at the discretion of the performing surgeon.
    Successful coagulation of all targeted vessels
    The rate of procedures with these fetoscopes in which there is successful coagulation of the targeted vessels will be studied. This measure will be at the discretion of the performing surgeon.
    The rate of preterm labor
    The rate of preterm labor following a procedure using these fetoscopes will be analyzed.
    The rate of preterm premature rupture of membranes (PPROM)
    The rate of PPROM following a procedure using these fetoscopes will be analyzed.
    The rate of placental abruption
    The rate of placental abruption following a procedure using these fetoscopes will be analyzed.
    The rate of choriamniotic separation (CAS)
    The rate of CAS following a procedure using these fetoscopes will be analyzed.
    The rate of iatrogenic septostomy
    The rate of iatrogenic septostomy following a procedure using these fetoscopes will be analyzed.
    The rate of completed Solomonizations
    The rate of completed Solomonizations (if clinically elected to be performed) during a procedure using these fetoscopes will be analyzed.
    The rate of any perioperative complications (within 24 hours post-procedure)
    The rate of any perioperative complications following a procedure using these fetoscopes will be analyzed.
    Fetal survival 48 hours post-procedure
    The rate of fetal survival at 48 hours following a procedure using these fetoscopes will be analyzed.
    Rate of TAPS
    In cases of twin-to-twin transfusion syndrome (TTTS) and selective fetal growth restriction (sFGR), the rate in which twin-anemia-polycythemia (TAPS) was observed following a procedure using these fetoscopes.
    Recurrence of TTTS
    In cases of twin-to-twin transfusion syndrome (TTTS), the rate in which TTTS recurred following a procedure using these fetoscopes.
    Neonatal survival 30 days after birth
    The rate of neonatal survival at 30 days of life following a procedure using these fetoscopes will be analyzed.
    Short term need for ECMO
    The rate of ECMO initiation during the first 30 days of life following a procedure using these fetoscopes will be analyzed.
    Short term morbidity
    The rate of short term morbidity during the first 30 days of life following a procedure using these fetoscopes will be analyzed. Short-term morbidity includes neurological problems, gastrointestinal problems, respiratory problems, infections, and other problems associated with prematurity including but not limited to: necrotizing enterocolitis, bronchopulmonary dysplasia, respiratory distress syndrome, neonatal sepsis, and neonatal intensive care unit admission.
    Gestational age at delivery
    Gestational age at delivery will be analyzed for study participants who undergo a procedure using these fetoscopes.
    Time from procedure to delivery
    Number of days from procedure to delivery will be analyzed for study participants who undergo a procedure using these fetoscopes.
    Length of procedure
    The length of time (in minutes) of the procedures using these fetoscopes will be analyzed.

    Full Information

    First Posted
    September 21, 2023
    Last Updated
    September 21, 2023
    Sponsor
    Boston Children's Hospital
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    1. Study Identification

    Unique Protocol Identification Number
    NCT06056635
    Brief Title
    A PROSPECTIVE STUDY ON THE ROLE OF KARL STORZ CURVED AND STRAIGHT FETOSCOPES (11508AAK and 11506AAK) FOR FETOSCOPIC INTRAUTERINE PROCEDURES
    Official Title
    A PROSPECTIVE STUDY ON THE ROLE OF KARL STORZ CURVED AND STRAIGHT FETOSCOPES (11508AAK and 11506AAK) FOR FETOSCOPIC INTRAUTERINE PROCEDURES
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    September 2023
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    December 1, 2023 (Anticipated)
    Primary Completion Date
    December 1, 2026 (Anticipated)
    Study Completion Date
    May 1, 2027 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Boston Children's Hospital

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    Yes
    Device Product Not Approved or Cleared by U.S. FDA
    Yes
    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    In this research study, we want to learn more about the role of new innovative surgical devices, the Karl Storz Curved and Straight Fetoscopes for in-utero surgery. A fetoscope is like a small telescope that can see inside of the uterus (womb) during minimally invasive surgery. The curved scope is used for patients with an anterior placenta (front of uterus), while the straight scope is used for patients with a posterior placenta (back of uterus). The scopes will be used to assist in procedures involving fetoscopic laser photocoagulation (FLP), which is a minimally invasive surgery that uses a small camera (fetoscope) to locate abnormal blood vessel connections in the placenta and seal them off using laser energy. These fetoscopes will be utilized in the diagnosis and management of various fetal conditions that can arise during pregnancy. Outcome data will be reported in a descriptive statistical analysis. We will assess the surgical outcomes, short and long-term morbidity, complications, and gestational age of these patients in order to evaluate the benefit of using these devices.
    Detailed Description
    The objective of this study is to evaluate the benefit of Karl Storz curved (11508AAK) and straight (11506AAK) fetoscopes for in-utero surgery. We will assess the surgical outcomes, short and long-term morbidity, complications, and gestational age of these patients. The scopes will be used to assist in intrauterine procedures across a variety of fetal conditions, such as TTTS (twin-twin transfusion syndrome), TAPS (twin anemia polycythemia sequence), sFGR (selective fetal growth restriction) or TRAP sequence (twin reversed arterial perfusion). Fetoscopic laser photocoagulation (FLP) can also be used during in-utero surgery to correct abnormal vessels in cases like chorioangioma or vasa previa. Other complex congenital anomalies may require fetal intervention or diagnostic fetoscopy using Storz scopes. Improvements in the technique, experience and equipment have been associated with better maternal, fetal, and neonatal outcomes in fetal surgery. Smaller fetoscopes are associated with lower rates of premature delivery following FLP. New fetoscopes (11508AAK and 11506AAK) have the potential to improve visualization and the photocoagulation angle. Compared to alternative scopes, these Storz scopes provide a wider angle of view and are longer, enabling better reach to distant areas at the edge of the placenta, especially in cases of higher BMI, higher gestational age, and significant polyhydramnios. This study is an un-blinded, non-randomized, single arm, feasibility study on a convenience cohort to demonstrate the role of a curved fetoscope device (11508AAK) or straight fetoscope device (11506AAK) among in-utero surgeries. Patients will be enrolled in a consecutive manner and all qualifying, patients who agreed to the use of the curved or straight fetoscopes will be enrolled in the study. Outcome data will be reported as a descriptive statistical analysis. The curved fetoscope (11508AAK) device will be used in monochorionic pregnancies with an anterior placenta requiring in-utero surgery, while the straight fetoscope (11506AAK) will be used in monochorionic pregnancies with a posterior placenta. This device is classified as a significant risk device because it is of substantial importance in diagnosing, curing, mitigating, or treating disease, or otherwise preventing impairment of human health and presents a potential for serious risk to the health, safety, or welfare of a subject.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Fetal Conditions, Maternal; Procedure, Pregnancy Related, Twin to Twin Transfusion Syndrome, In Utero Procedure Affecting Fetus or Newborn, Chorion; Abnormal, Twin Reversal Arterial Perfusion Syndrome, Twin Monochorionic Monoamniotic Placenta, Chorioangioma, Vasa Previa
    Keywords
    Fetoscope, Fetoscopic Laser Ablation, Diagnostic Fetoscopy

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Single Group Assignment
    Masking
    None (Open Label)
    Allocation
    N/A
    Enrollment
    50 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Karl Storz Curved or Straight Scope
    Arm Type
    Experimental
    Arm Description
    A Karl Storz Curved (11508AAK) or Straight (11506AAK) Fetoscope will be used to provide visualization during in-utero (in the womb) diagnostic and interventional procedures. The curved scope will be used in patients with a placenta that sits at the front of their uterus. The straight scope will be used in patients with a placenta that sits at the back of their uterus.
    Intervention Type
    Device
    Intervention Name(s)
    Karl Storz Curved (11508AAK) and Straight (11506AAK) Fetoscopes
    Intervention Description
    These fetoscopes will be used to view target areas during in-utero procedures. There are various fetal conditions that may require use of a fetoscope during minimally invasive surgery. These include the need to seal vessels in order to stop blood flow going in a specific direction during pregnancy, abnormal vessels that may need to be sealed, or to break down scar tissue, extra tissue attachments, or blockages.
    Primary Outcome Measure Information:
    Title
    Rate of completed fetoscopic procedures
    Description
    The rate of successfully completed intrauterine procedures (out of 50 total) using the Karl Storz Curved (11508AAK) or Straight (11506AAk) Fetoscope will be measured.
    Time Frame
    3 years from study start date
    Title
    Fetal survival at birth
    Description
    The number of fetuses who undergo an intrauterine fetoscopic procedure using these devices and survive at birth will be analyzed.
    Time Frame
    When the last (50th) study participant reaches birth. Likely to be a bit more than 3 years from study start date.
    Secondary Outcome Measure Information:
    Title
    Successful visualization of all targeted vessels
    Description
    The rate of procedures with these fetoscopes in which there is successful visualization of the targeted vessels will be studied. This measure will be at the discretion of the performing surgeon.
    Time Frame
    3 years from study start date
    Title
    Successful coagulation of all targeted vessels
    Description
    The rate of procedures with these fetoscopes in which there is successful coagulation of the targeted vessels will be studied. This measure will be at the discretion of the performing surgeon.
    Time Frame
    3 years from study start date
    Title
    The rate of preterm labor
    Description
    The rate of preterm labor following a procedure using these fetoscopes will be analyzed.
    Time Frame
    When the last (50th) study participant reaches birth. This is likely to be a bit longer than 3 years from study start date.
    Title
    The rate of preterm premature rupture of membranes (PPROM)
    Description
    The rate of PPROM following a procedure using these fetoscopes will be analyzed.
    Time Frame
    When the last (50th) study participant reaches birth. This is likely to be a bit longer than 3 years from study start date.
    Title
    The rate of placental abruption
    Description
    The rate of placental abruption following a procedure using these fetoscopes will be analyzed.
    Time Frame
    When the last (50th) study participant reaches birth. This is likely to be a bit longer than 3 years from study start date.
    Title
    The rate of choriamniotic separation (CAS)
    Description
    The rate of CAS following a procedure using these fetoscopes will be analyzed.
    Time Frame
    When the last (50th) study participant reaches birth. This is likely to be a bit longer than 3 years from study start date.
    Title
    The rate of iatrogenic septostomy
    Description
    The rate of iatrogenic septostomy following a procedure using these fetoscopes will be analyzed.
    Time Frame
    When the last (50th) study participant reaches birth. This is likely to be a bit longer than 3 years from study start date.
    Title
    The rate of completed Solomonizations
    Description
    The rate of completed Solomonizations (if clinically elected to be performed) during a procedure using these fetoscopes will be analyzed.
    Time Frame
    3 years from study start date
    Title
    The rate of any perioperative complications (within 24 hours post-procedure)
    Description
    The rate of any perioperative complications following a procedure using these fetoscopes will be analyzed.
    Time Frame
    24 hours after the last (50th) procedure using these fetoscopes. This will be a bit more than 3 years from study start date.
    Title
    Fetal survival 48 hours post-procedure
    Description
    The rate of fetal survival at 48 hours following a procedure using these fetoscopes will be analyzed.
    Time Frame
    24 hours after the last (50th) procedure using these fetoscopes. This will be a bit more than 3 years from study start date.
    Title
    Rate of TAPS
    Description
    In cases of twin-to-twin transfusion syndrome (TTTS) and selective fetal growth restriction (sFGR), the rate in which twin-anemia-polycythemia (TAPS) was observed following a procedure using these fetoscopes.
    Time Frame
    When the last (50th) study participant reaches birth. This is likely to be a bit longer than 3 years from study start date.
    Title
    Recurrence of TTTS
    Description
    In cases of twin-to-twin transfusion syndrome (TTTS), the rate in which TTTS recurred following a procedure using these fetoscopes.
    Time Frame
    When the last (50th) study participant reaches birth. This is likely to be a bit longer than 3 years from study start date.
    Title
    Neonatal survival 30 days after birth
    Description
    The rate of neonatal survival at 30 days of life following a procedure using these fetoscopes will be analyzed.
    Time Frame
    When the last (50th) study participant reaches 30 days post-birth. This is likely to be a bit longer than 3 years from study start date.
    Title
    Short term need for ECMO
    Description
    The rate of ECMO initiation during the first 30 days of life following a procedure using these fetoscopes will be analyzed.
    Time Frame
    When the last (50th) study participant reaches 30 days post-birth. This is likely to be a bit longer than 3 years from study start date.
    Title
    Short term morbidity
    Description
    The rate of short term morbidity during the first 30 days of life following a procedure using these fetoscopes will be analyzed. Short-term morbidity includes neurological problems, gastrointestinal problems, respiratory problems, infections, and other problems associated with prematurity including but not limited to: necrotizing enterocolitis, bronchopulmonary dysplasia, respiratory distress syndrome, neonatal sepsis, and neonatal intensive care unit admission.
    Time Frame
    When the last (50th) study participant reaches 30 days post-birth. This is likely to be a bit longer than 3 years from study start date.
    Title
    Gestational age at delivery
    Description
    Gestational age at delivery will be analyzed for study participants who undergo a procedure using these fetoscopes.
    Time Frame
    When the last (50th) study participant reaches birth. This is likely to be a bit longer than 3 years from study start date.
    Title
    Time from procedure to delivery
    Description
    Number of days from procedure to delivery will be analyzed for study participants who undergo a procedure using these fetoscopes.
    Time Frame
    When the last (50th) study participant reaches birth. This is likely to be a bit longer than 3 years from study start date.
    Title
    Length of procedure
    Description
    The length of time (in minutes) of the procedures using these fetoscopes will be analyzed.
    Time Frame
    3 years from study start date

    10. Eligibility

    Sex
    Female
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    45 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Pregnant patient with a condition requiring in-utero surgery Patient must be eligible for anesthesia Patient and father of the fetus (if available) are able to provide signed informed consent Exclusion Criteria: Allergy or previous adverse reaction to any ancillary medication specified in this protocol that has no alternative Preterm labor, preeclampsia, or uterine anomaly (e.g., large fibroid tumor) in the index pregnancy Suspicion of major recognized congenital syndrome on ultrasound or MRI that is not compatible with postnatal life Pre-pregnancy maternal BMI greater than 40 High risk for fetal hemophilia Fetal aneuploidy or variants of known significance if an amniocentesis was performed Contraindication to abdominal surgery or fetoscopic surgery
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Brittany Gudanowski
    Phone
    617-919-6658
    Email
    Brittany.Gudanowski@childrens.harvard.edu
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Eyal Krispin, MD
    Organizational Affiliation
    Boston Children's Hospital
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No
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    A PROSPECTIVE STUDY ON THE ROLE OF KARL STORZ CURVED AND STRAIGHT FETOSCOPES (11508AAK and 11506AAK) FOR FETOSCOPIC INTRAUTERINE PROCEDURES

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