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A Prospective Study of Misoprostol Administration in Asymptomatic Patients With Pregnancies of Unknown Location

NCT02581761 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 100

Last updated 2015-10-21

No results posted yet for this study

Summary

A randomized prospective double blind study of misoprostol administration in asymptomatic patients with pregnancies of unknown location.

Conditions

  • Pregnancies of Unknown Location (PUL)

Interventions

DRUG

CYTOTEC

synthetic prostaglandin E1

OTHER

Placebo

no active material

Sponsors & Collaborators

  • Sheba Medical Center

    lead OTHER_GOV

Study Design

Allocation
RANDOMIZED
Purpose
DIAGNOSTIC
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2015-11-30
Primary Completion
2017-11-30
Completion
2018-03-31

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02581761 on ClinicalTrials.gov