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NCT01937988 · ClinicalTrials.gov registry record · NA
Patient Support During Surgical Abortion
A NA study, sponsored by University of Chicago.
- Completed
- Registry status
- NA
- Development phase
- 220
- Enrollment target
NCT01937988 is a NA study that has completed, run by University of Chicago. The registered enrollment target is 220 participants.
The verdict
NCT01937988, a NA study, has completed, sponsored by University of Chicago.
- COMPLETED
- Registry status
- NA
- Development phase
- 220 participants
- Enrollment target
Study Summary
This study will be a non-blinded randomized controlled trial (RCT) of women presenting for abortion at \<13 6/7 weeks. Women will be randomized either to receive support by a trained abortion doula (intervention) or to have standard procedure (control) during the abortion procedure. The investigators hypothesize that women who receive doula support during a first trimester abortion will report less pain during the abortion procedure compared to women who do not receive abortion doula support.
Interventions
- OTHER Doula Arm
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 220 participants |
| Start Date | 2013-05 |
| Est. Completion | 2013-07 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01937988
The ClinicalTrials.gov registry entry for NCT01937988 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 220 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Chicago, which has 796 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which Doula Arm is the first listed.
NCT01937988 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01937988 about?
NCT01937988 is a clinical study titled "Patient Support During Surgical Abortion". This study will be a non-blinded randomized controlled trial (RCT) of women presenting for abortion at \<13 6/7 weeks. Women will be randomized either to receive support by a trained abortion doula (intervention) or to have standard procedure (control) during the abortion procedure. The investigator...
What is the current status of trial NCT01937988?
This trial is currently completed. It is a NA study. The enrollment target is 220 participants. The study started on 2013-05. Estimated completion is 2013-07.
What interventions are being tested in trial NCT01937988?
The interventions under investigation include: Doula Arm (OTHER).
Who is sponsoring clinical trial NCT01937988?
This trial is sponsored by University of Chicago, which has 796 total clinical trials registered on ClinicalTrials.gov.
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