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Efficacy of Expectant Management for Preterm Subclinical Intra-Amniotic Infection

Efficacy of Expectant Management for Preterm Subclinical Intra-Amniotic Infection - Expectant Management for Intra-Amniotic Infection

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000059353
Enrollment
42
Registered
2026-03-31
Start date
2025-02-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Preterm Subclinical Intra-Amniotic Infection

Interventions

None listed

Sponsors

NHO Saga Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: (1) singleton gestation between 20+0 and 33+6 weeks; (2) transabdominal amniocentesis performed to assess microbiological and inflammatory status of the amniotic cavity; (3) diagnosis of intra-amniotic infection; and (4) expectant management.

Exclusion criteria

Exclusion criteria: (1) decision to terminate pregnancy after a diagnosis of intra-amniotic infection; (2) antimicrobial administration within seven days prior to amniocentesis; (3) secondary intra-amniotic infection; (4) fetal congenital structural or chromosomal abnormalities; and (5) induction of labor within 48 h of infection diagnosis due to oligohydramnios or infection itself.

Design outcomes

Primary

MeasureTime frame
the proportion of patients in which the interval from the diagnosis of infection to delivery exceeded 48 h without exacerbation of IAI, as compared between the U/Mh-only and other bacteria groups.

Secondary

MeasureTime frame
Secondary outcome was assessed at the same interval, but extended to 168 h.

Countries

Japan

Contacts

Public ContactMakoto Nomiyama

NHO Saga Hospital Department of Obstetrics and Gynecology

nomiyama8522@gmail.com0952307141

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026