NCT03243513

Brief Summary

The aim of the project is to identify an efficient and effective policy or procedure for identifying complications from surgical abortions through follow-up phone calls.

Trial Health

57
Monitor

Trial Health Score

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

Enrollment
1,600

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Aug 2017

Typical duration for all trials

Geographic Reach
1 country

1 active site

Status
terminated

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

First Submitted

Initial submission to the registry

August 4, 2017

Completed
Same day until next milestone

Study Start

First participant enrolled

August 4, 2017

Completed
5 days until next milestone

First Posted

Study publicly available on registry

August 9, 2017

Completed
2.6 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 28, 2020

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

February 28, 2020

Completed
Last Updated

January 12, 2024

Status Verified

January 1, 2024

Enrollment Period

2.6 years

First QC Date

August 4, 2017

Last Update Submit

January 10, 2024

Conditions

Outcome Measures

Primary Outcomes (1)

  • Follow-up Phone Calls

    Key questions include, what is our complication-detection rate from these phone calls? How many patients are contacted? How many attempts are made and how much effort is expended by staff in routine follow-up practices?

    2 years

Interventions

There is no intervention in this research. This research project is a retrospective chart review.

Eligibility Criteria

Sexfemale
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

De-identified charts of women who have had an induced abortion and are contacted by a nurse for a follow-up phone call.

You may qualify if:

  • Reproductive-aged women
  • women who have had an induced abortion, and are contacted by a clinical nurse for a follow-up phone call.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of New Mexico

Albuquerque, New Mexico, 87131, United States

Location

Study Officials

  • Lisa Hofler, MD, MBA, MPH

    University of New Mexico

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant Professor

Study Record Dates

First Submitted

August 4, 2017

First Posted

August 9, 2017

Study Start

August 4, 2017

Primary Completion

February 28, 2020

Study Completion

February 28, 2020

Last Updated

January 12, 2024

Record last verified: 2024-01

Data Sharing

IPD Sharing
Will not share

We do not plan on sharing IPD at this time

Locations