- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT07620613
Perinatal Mortality Outcomes Through Household Infection Pathways (POTH)
Effect of Cement Floors on Perinatal and Neonatal Mortality in Bangladesh: a Randomized Trial in Rural Bangladesh
The goal of this trial is to learn if replacing household soil floors with concrete floors can prevent deaths of infants around the time of birth, including stillbirths and deaths in the first month of life in rural Bangladesh. The primary question the study aims to answer is: Does residing in a home with a concrete vs. soil floor reduce the perinatal and neonatal morality in index children and their younger siblings up to 6 years post-installation of concrete floors?
Researchers will compare participants in households with concrete floors (intervention) vs. soil floors (comparison group) to see if concrete floors reduce the rate of perinatal death and child death up the 6 years post-intervention.
This study will extend an ongoing NIH-funded randomized trial in which households with soil floors where a pregnant woman resided were randomly chosen to receive a concrete floor intervention or to retain their existing soil floor. This study will track pregnancies, births, and deaths among infants born to pregnant mothers in the original study to measure effects of household concrete flooring up to 6 years after the concrete floors were installed.
Studieoversikt
Status
Intervensjon / Behandling
Detaljert beskrivelse
Studietype
Registrering (Antatt)
Fase
- Ikke aktuelt
Kontakter og plasseringer
Studiesteder
-
-
-
Dhaka, Bangladesh
- International Centre for Diarrhoeal Disease Research, Bangladesh
-
Hovedetterforsker:
- Md. Mahbubur Rahman, MBBS
-
-
Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
- Barn
Tar imot friske frivillige
Beskrivelse
Inclusion Criteria:
- Prior enrollment in the CRADLE trial (NCT05372068), in either arm, and currently residing in the original CRADLE-enrolled household
- Residence in Sirajganj or Tangail districts in Bangladesh
- No major non-compliance (e.g., no removal of concrete floor in intervention arm or installation of concrete floor in control arm)
- No plan to relocate within the study follow-up period
- Incident pregnancy occurring after CRADLE trial enrollment, confirmed after 26 weeks gestation
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Forebygging
- Tildeling: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Enkelt
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Ingen inngripen: Ikke-intervensjon
|
|
|
Eksperimentell: Concrete household floor
Household soil floors will be replaced with concrete floors
|
Husholdningsjordgulv vil bli erstattet med betonggulv
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Extended perinatal mortality rate
Tidsramme: Up to 6 years post-intervention delivery in parent study
|
Total number of stillbirths (babies born following fetal deaths at 22 weeks or later gestation) and neonatal deaths within the first 28 days after birth divided by the number of total births (live births + stillbirths)
|
Up to 6 years post-intervention delivery in parent study
|
Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Stillbirth rate
Tidsramme: Up to 6 years post-intervention delivery in parent study
|
Total number of stillbirths (babies born following fetal deaths at 22 weeks or later gestation) divided by the number of total births (live births + stillbirths)
|
Up to 6 years post-intervention delivery in parent study
|
|
Early neonatal mortality rate
Tidsramme: Up to 6 years post-intervention delivery in parent study
|
Total number of deaths occurring in the first 7 days of life divided by the number of live births
|
Up to 6 years post-intervention delivery in parent study
|
|
Neonatal mortality rate
Tidsramme: Up to 6 years post-intervention delivery in parent study
|
Total number of deaths occurring in the first 28 days of life divided by the number of live births
|
Up to 6 years post-intervention delivery in parent study
|
|
Infant mortality rate
Tidsramme: Up to 6 years post-intervention delivery in parent study
|
Total deaths prior to age 12 months among live births divided by total live births
|
Up to 6 years post-intervention delivery in parent study
|
|
Child mortality rate
Tidsramme: Up to 6 years post-intervention delivery in parent study
|
Total deaths at any age among live births divided by total live births
|
Up to 6 years post-intervention delivery in parent study
|
Samarbeidspartnere og etterforskere
Sponsor
Samarbeidspartnere
Etterforskere
- Hovedetterforsker: Jade Benjamin-Chung, PhD MPH, Stanford University
Publikasjoner og nyttige lenker
Hjelpsomme linker
Studierekorddatoer
Studer hoveddatoer
Studiestart (Antatt)
Primær fullføring (Antatt)
Studiet fullført (Antatt)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Faktiske)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- 86289
- 03001 (Annet stipend/finansieringsnummer: Thrasher Foundation)
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
IPD-planbeskrivelse
IPD-delingstidsramme
Tilgangskriterier for IPD-deling
IPD-deling Støtteinformasjonstype
- STUDY_PROTOCOL
- SEVJE
- ANALYTIC_CODE
Legemiddel- og utstyrsinformasjon, studiedokumenter
Studerer et amerikansk FDA-regulert medikamentprodukt
Studerer et amerikansk FDA-regulert enhetsprodukt
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