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Pain Control In First Trimester Medical Abortion: A Randomized Trial

NCT01457521 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 250

Last updated 2016-01-13

Study results available
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Summary

This trial will compare two oral analgesic regimens in women undergoing first trimester medical abortion with mifepristone and misoprostol. The primary study outcome is pain.

Conditions

Interventions

DRUG

Ibuprofen

Ibuprofen

Sponsors & Collaborators

  • Society of Family Planning

    collaborator OTHER

  • Family Planning Associates Medical Group, LTD

    collaborator OTHER

  • Planned Parenthood of Greater New York

    collaborator OTHER

  • Gynuity Health Projects

    lead OTHER

Principal Investigators

  • Elizabeth Raymond, MD, MPH · Gynuity Health Projects

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-10-31
Primary Completion
2012-12-31
Completion
2012-12-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Drugs
Diseases
Companies

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 NCT01457521 on ClinicalTrials.gov