Prenatal Steroids for Treatment of Congenital Cystic Adenomatoid Malformations (CCAM) (CCAM Steroids)
Primary Purpose
Congenital Cystic Adenomatoid Malformation
Status
Terminated
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Betamethasone
Placebo
Sponsored by
About this trial
This is an interventional prevention trial for Congenital Cystic Adenomatoid Malformation focused on measuring prenatal steroids, hydrops, congenital cystic adenomatoid malformation of the lung, prenatal intervention, betamethasone, prenatal diagnosis
Eligibility Criteria
Inclusion Criteria:
- GA < 26 weeks
- Maternal age > 18 years of age
- Singleton pregnancy
- Normal chromosomes
- CCAM volume to head circumference ratio (CVR) > 1.4
- No maternal medical/surgical contraindications
- No evidence of hydrops
- Not previously randomization
Exclusion Criteria:
- Maternal diabetes or use of insulin
- Preterm labor
- Multiple congenital anomalies with CCAM
- Chromosomal anomaly with CCAM
- Multiple gestation pregnancy with CCAM
- Not willing to be randomized
- Unable or unwilling to return to UCSF for second dose of drug or placebo
- CVR < 1.4
Sites / Locations
- University of California, San Francisco Fetal Treatment Center
- Cincinnati Children's Hospital
- Children's Hospital of Philadelphia
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Placebo Comparator
Arm Label
Active Study Group
Placebo Group
Arm Description
STEROID: Betamethasone; 12 mg intramuscularly x 2 doses 24 hours apart
PLACEBO: IM x 2 doses 24 hours apart
Outcomes
Primary Outcome Measures
Incidence of Hydrops Fetalis
Secondary Outcome Measures
Comparison of CCAM Size in Mid-trimester Fetuses (Study/Administration vs Control/Placebo)
Survival at One-month Between Study and Control Groups.
Status of neonate survival 30 days after delivery
Full Information
NCT ID
NCT00670956
First Posted
April 30, 2008
Last Updated
March 18, 2015
Sponsor
University of California, San Francisco
Collaborators
Children's Hospital Medical Center, Cincinnati, Children's Hospital of Philadelphia
1. Study Identification
Unique Protocol Identification Number
NCT00670956
Brief Title
Prenatal Steroids for Treatment of Congenital Cystic Adenomatoid Malformations (CCAM)
Acronym
CCAM Steroids
Official Title
Investigation of Prenatal Steroids for Treatment of Prenatally Diagnosed CCAMs
Study Type
Interventional
2. Study Status
Record Verification Date
March 2015
Overall Recruitment Status
Terminated
Why Stopped
Recruitment has been poor. Study drug is being offered as part of standard care of women carrying a pregnancy diagnosed with CCAM
Study Start Date
April 2008 (undefined)
Primary Completion Date
September 2011 (Actual)
Study Completion Date
September 2011 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of California, San Francisco
Collaborators
Children's Hospital Medical Center, Cincinnati, Children's Hospital of Philadelphia
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Congenital cystic adenomatoid malformations (CCAMs) are theorized to be growing immature lung tissue. Administration of maternal steroids in the mid-trimester may stop the growth or decrease the size of the CCAM, thus increasing normal lung tissue and improving survival in fetuses with large CCAMs. This is a prospective, blinded, randomized trial comparing administration of a single course of antenatal steroids (Betamethasone) to control (i.e., placebo). The primary outcome variable will be incidence of hydrops. One month postnatal survival and relative size of the CCAM as determined by CCAM volume:head circumference ratio (CVR) between treatment/no treatment groups will be secondary outcome variables. Change in size of CCAM will be serially followed for both groups with individual growth curves being plotted prenatally and these will be compared with pathology weigh and volume to evaluate treatment effect. Other prenatal data collected will include: incidence of polyhydramnios, incidence of premature rupture of membranes, incidence of material complications. We will also compare mode of delivery, postnatal respiratory compromise, need for resection in the first week of life, and occurrence of complications during newborn administration
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Congenital Cystic Adenomatoid Malformation
Keywords
prenatal steroids, hydrops, congenital cystic adenomatoid malformation of the lung, prenatal intervention, betamethasone, prenatal diagnosis
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 1, Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
1 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Active Study Group
Arm Type
Active Comparator
Arm Description
STEROID: Betamethasone; 12 mg intramuscularly x 2 doses 24 hours apart
Arm Title
Placebo Group
Arm Type
Placebo Comparator
Arm Description
PLACEBO: IM x 2 doses 24 hours apart
Intervention Type
Drug
Intervention Name(s)
Betamethasone
Intervention Description
12 mg intramuscularly x 2 doses 24 hours apart
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
PLACEBO: IM x 2 doses 24 hours apart
Primary Outcome Measure Information:
Title
Incidence of Hydrops Fetalis
Time Frame
Delivery, up to approximately 20 weeks post-enrollment
Secondary Outcome Measure Information:
Title
Comparison of CCAM Size in Mid-trimester Fetuses (Study/Administration vs Control/Placebo)
Time Frame
Baseline, Delivery (up to approximately 20 weeks post-enrollment)
Title
Survival at One-month Between Study and Control Groups.
Description
Status of neonate survival 30 days after delivery
Time Frame
30 days after delivery (up to approximately 24 weeks post-enrollment)
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
GA < 26 weeks
Maternal age > 18 years of age
Singleton pregnancy
Normal chromosomes
CCAM volume to head circumference ratio (CVR) > 1.4
No maternal medical/surgical contraindications
No evidence of hydrops
Not previously randomization
Exclusion Criteria:
Maternal diabetes or use of insulin
Preterm labor
Multiple congenital anomalies with CCAM
Chromosomal anomaly with CCAM
Multiple gestation pregnancy with CCAM
Not willing to be randomized
Unable or unwilling to return to UCSF for second dose of drug or placebo
CVR < 1.4
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Timothy M Crombleholme, MD
Organizational Affiliation
Children's Hospital of Cincinnati
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Douglas Wilson, MD
Organizational Affiliation
Children's Hospital of Philadelphia
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Hanmin Lee, MD
Organizational Affiliation
University of California, San Francisco
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of California, San Francisco Fetal Treatment Center
City
San Francisco
State/Province
California
ZIP/Postal Code
94143
Country
United States
Facility Name
Cincinnati Children's Hospital
City
Cincinnati
State/Province
Ohio
ZIP/Postal Code
45229-3039
Country
United States
Facility Name
Children's Hospital of Philadelphia
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19104
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
17706495
Citation
Vu L, Tsao K, Lee H, Nobuhara K, Farmer D, Harrison M, Goldstein RB. Characteristics of congenital cystic adenomatoid malformations associated with nonimmune hydrops and outcome. J Pediatr Surg. 2007 Aug;42(8):1351-6. doi: 10.1016/j.jpedsurg.2007.03.039.
Results Reference
background
PubMed Identifier
17099841
Citation
Schumacher A, Sidor J, Buhling KJ. [Continuous glucose monitoring using the glucose sensor CGMS in metabolically normal pregnant women during betamethasone therapy for fetal respiratory distress syndrome]. Z Geburtshilfe Neonatol. 2006 Oct;210(5):184-90. doi: 10.1055/s-2006-951743. German.
Results Reference
background
PubMed Identifier
17272618
Citation
Peltoniemi OM, Kari MA, Tammela O, Lehtonen L, Marttila R, Halmesmaki E, Jouppila P, Hallman M; Repeat Antenatal Betamethasone Study Group. Randomized trial of a single repeat dose of prenatal betamethasone treatment in imminent preterm birth. Pediatrics. 2007 Feb;119(2):290-8. doi: 10.1542/peds.2006-1549.
Results Reference
background
PubMed Identifier
16856047
Citation
Roberts D, Dalziel S. Antenatal corticosteroids for accelerating fetal lung maturation for women at risk of preterm birth. Cochrane Database Syst Rev. 2006 Jul 19;(3):CD004454. doi: 10.1002/14651858.CD004454.pub2.
Results Reference
background
PubMed Identifier
17233108
Citation
Neilson JP. Antenatal corticosteroids for accelerating fetal lung maturation for women at risk of preterm birth. Obstet Gynecol. 2007 Jan;109(1):189-90. doi: 10.1097/01.aog.0000251610.51286.b1. No abstract available.
Results Reference
background
PubMed Identifier
12632377
Citation
Tsao K, Hawgood S, Vu L, Hirose S, Sydorak R, Albanese CT, Farmer DL, Harrison MR, Lee H. Resolution of hydrops fetalis in congenital cystic adenomatoid malformation after prenatal steroid therapy. J Pediatr Surg. 2003 Mar;38(3):508-10. doi: 10.1053/jpsu.2003.50089.
Results Reference
background
PubMed Identifier
15325542
Citation
Arca MJ, Teich S. Current controversies in perinatal care: fetal versus neonatal surgery. Clin Perinatol. 2004 Sep;31(3):629-48. doi: 10.1016/j.clp.2004.03.016.
Results Reference
background
PubMed Identifier
15305098
Citation
Wilson RD, Baxter JK, Johnson MP, King M, Kasperski S, Crombleholme TM, Flake AW, Hedrick HL, Howell LJ, Adzick NS. Thoracoamniotic shunts: fetal treatment of pleural effusions and congenital cystic adenomatoid malformations. Fetal Diagn Ther. 2004 Sep-Oct;19(5):413-20. doi: 10.1159/000078994.
Results Reference
background
PubMed Identifier
17001747
Citation
Knox EM, Kilby MD, Martin WL, Khan KS. In-utero pulmonary drainage in the management of primary hydrothorax and congenital cystic lung lesion: a systematic review. Ultrasound Obstet Gynecol. 2006 Oct;28(5):726-34. doi: 10.1002/uog.3812.
Results Reference
background
PubMed Identifier
15065026
Citation
Davenport M, Warne SA, Cacciaguerra S, Patel S, Greenough A, Nicolaides K. Current outcome of antenally diagnosed cystic lung disease. J Pediatr Surg. 2004 Apr;39(4):549-56. doi: 10.1016/j.jpedsurg.2003.12.021.
Results Reference
background
PubMed Identifier
8783108
Citation
Miller JA, Corteville JE, Langer JC. Congenital cystic adenomatoid malformation in the fetus: natural history and predictors of outcome. J Pediatr Surg. 1996 Jun;31(6):805-8. doi: 10.1016/s0022-3468(96)90138-4.
Results Reference
background
Links:
URL
http://www.fetalcarecenter.org/
Description
Fetal Care Center of Cincinnati Children's Hospital
URL
http://fetus.ucsfmedicalcenter.org/
Description
Fetal Treatment Center at the University of California, San Francisco
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Prenatal Steroids for Treatment of Congenital Cystic Adenomatoid Malformations (CCAM)
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