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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03079622
Other study ID # 1.0
Secondary ID
Status Completed
Phase N/A
First received November 18, 2015
Last updated March 7, 2017
Start date November 2015
Est. completion date June 2016

Study information

Verified date March 2017
Source Washington University School of Medicine
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The study titled, Manual Versus Electric Vacuum Aspiration for Pregnancy Termination Between 10-14 weeks: A Randomized Trial, is a randomized trial to compare procedure times for manual and electric vacuum aspiration for surgical abortion between 10 0/7 and 13 6/7 weeks gestation. Women presenting for surgical abortion between 10 0/7 and 13 6/7 weeks gestation will be randomized to either undergo manual vacuum aspiration (MVA) or electric vacuum aspiration (EVA). The investigators hypothesize that operative times will be increased when using manual vacuum aspiration, as compared to electric vacuum aspiration, for surgical abortion performed in the late first trimester (10 0/7 and-13 6/7 weeks).


Recruitment information / eligibility

Status Completed
Enrollment 146
Est. completion date June 2016
Est. primary completion date June 2016
Accepts healthy volunteers No
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Between 10 0/7 and 13 6/7 weeks of gestation

- Documented intra-uterine pregnancy

- Presenting for surgical induced abortion at RHS

- English-speaking

- Age 18 or older

Exclusion Criteria:

- Spontaneous abortion

- Failed medical abortion

- Multiple gestation

- Uterine anomalies

- Lower uterine segment or cervical myomas

- History of 3 or more prior cesarean deliveries

- BMI > 40

- Having the abortion procedure performed by a provider who does not perform MVA and EVA between 10 0/7 and 13 6/7 weeks

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Electric Vacuum Aspiration

Manual Vacuum Aspiration


Locations

Country Name City State
United States Washington University in St. Louis Saint Louis Missouri

Sponsors (1)

Lead Sponsor Collaborator
Washington University School of Medicine

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Operative time Time from cannula insertion until completion of uterine evacuation Perioperative
Secondary Conversion from electric to manual vacuum aspiration (or vice versa) during the procedure Perioperative
Secondary Provider acceptability 1) Ease of procedure on a 5 point Likert scale, 2) Appropriateness of method used for procedure (binary response) Perioperative
Secondary Patient acceptability 1) Satisfaction with procedure on 4-point rating scale 2) Would choose same procedure again (binary response) 3) Would recommend procedure to a friend (binary response) Perioperative and 2 weeks postoperatively
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