NCT00357526

Brief Summary

The purpose of this study is to determine whether teens and young women would prefer the Nuvaring to oral contraceptive pills after having tried both methods.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
130

participants targeted

Target at P50-P75 for not_applicable pregnancy

Timeline
Completed

Started Apr 2003

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

April 1, 2003

Completed
1.3 years until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2004

Completed
2 years until next milestone

First Submitted

Initial submission to the registry

July 25, 2006

Completed
2 days until next milestone

First Posted

Study publicly available on registry

July 27, 2006

Completed
Last Updated

April 23, 2007

Status Verified

March 1, 2006

First QC Date

July 25, 2006

Last Update Submit

April 19, 2007

Conditions

Pregnancy

Keywords

vaginal ringOral contraceptive pillsTeenagersYoung womenPatient satisfaction

Outcome Measures

Primary Outcomes (1)

  • Satisfaction

Secondary Outcomes (2)

  • Compliance

  • Acceptability

Interventions

OCPsDRUG
vaginal ringDEVICE

Eligibility Criteria

Age15 Years - 21 Years
Sexfemale
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64)

You may qualify if:

  • Sexually active young women (n=130), English or Spanish speaking, aged 15-21 years, able and willing to try oral contraceptives and vaginal rings for 6 months

You may not qualify if:

  • Not able or willing to use hormonal contraceptives, moving out of the area, pregnant or intending to become pregnant during the study time frame, not sexually active

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

New Generation Health Center

San Francisco, California, 94110, United States

Location

MeSH Terms

Conditions

Patient Satisfaction

Interventions

Contraceptive Devices, Female

Condition Hierarchy (Ancestors)

Treatment Adherence and ComplianceHealth BehaviorBehavior

Intervention Hierarchy (Ancestors)

Contraceptive DevicesEquipment and Supplies

Study Officials

  • Felicia Stewart, MD

    University of California, San Francisco

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
CROSSOVER
Sponsor Type
OTHER

Study Record Dates

First Submitted

July 25, 2006

First Posted

July 27, 2006

Study Start

April 1, 2003

Study Completion

August 1, 2004

Last Updated

April 23, 2007

Record last verified: 2006-03

Locations

US(1)