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Mifepristone Versus Laminaria for Cervical Ripening in Midtrimester Induction

Randomized Controlled Trial of Mifepristone Versus Laminaria for Cervical Ripening In Midtrimester Induction

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00383032
Enrollment
72
Registered
2006-10-02
Start date
2004-01-31
Completion date
2006-06-30
Last updated
2023-10-24

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

Conditions

Abortion, Induced

Brief summary

Data from other countries have suggested that oral mifepristone used as a cervical ripening agent may decrease induction to delivery time in midtrimester inductions. To our knowledge, there are no trials comparing mifepristone to laminaria in a standard clinical setting with standardized misoprostol induction protocol to examine the issue of induction to delivery time. We hypothesize that mifepristone will work at least as well as laminaria for midtrimester cervical ripening prior to induction of labor with misoprostol.

Interventions

DRUGmifepristone

Sponsors

Dartmouth-Hitchcock Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
16 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* pregnant women with fetal anomalies, aneuploidy, or demise at 15-22 weeks gestation * age greater than 16 * able to speak English

Exclusion criteria

* prior uterine scar or * allergy or history of bad reaction to any of the study drugs or * history of chronic adrenal failure or * porphyria or * concurrent long-term corticosteroid treatment

Design outcomes

Primary

MeasureTime frame
induction to delivery time

Secondary

MeasureTime frame
pain
delivery within 24 hours
need for post-partum D&C
adverse events

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026