Abortion in First Trimester Clinical Trial
Official title:
Manual Versus Electric Vacuum Aspiration for Pregnancy Termination Between 10-14 Weeks: A Randomized Trial
Verified date | March 2017 |
Source | Washington University School of Medicine |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
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).
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 |
Country | Name | City | State |
---|---|---|---|
United States | Washington University in St. Louis | Saint Louis | Missouri |
Lead Sponsor | Collaborator |
---|---|
Washington University School of Medicine |
United States,
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 |
Status | Clinical Trial | Phase | |
---|---|---|---|
Terminated |
NCT04056637 -
Choice of Modality of Follow up for Medication Abortion
|
N/A | |
Active, not recruiting |
NCT05896657 -
Modulation of Reproductive Microbiota by Ligilactobacillus Salivarius CECT5713
|
N/A | |
Active, not recruiting |
NCT03736681 -
Effect of Paracervical Block Volume on Pain Control for Dilation and Curettage
|
Phase 1 | |
Completed |
NCT03636451 -
Effect of Paracervical Block Volume on Pain Control for Dilation and Curettage.o
|
Phase 3 | |
Completed |
NCT04446572 -
Application of Lactobacillus Salivarius CECT5713 in Infertility of Unknown Origin
|
Phase 2 | |
Not yet recruiting |
NCT03267771 -
Progesterone and Doppler in Recurrent Abortion
|
Phase 4 | |
Recruiting |
NCT05341817 -
The Use of Letrozole or Mifepristone for Pretreatment of Medical Termination of Pregnancy
|
Phase 4 | |
Recruiting |
NCT05182008 -
A Patient Decision Aid for Method of Early Abortion: A Randomized Control Trial
|
N/A | |
Completed |
NCT03417362 -
Delivery of Audiovisual Information on Early Medical Abortion
|
N/A | |
Completed |
NCT03896022 -
Auriculotherapy - Pain Management of Aspiration Abortion
|
N/A | |
Completed |
NCT03925129 -
Transcutaneous Electrical Nerve Stimulation (TENS) for Pain Management With Medication Abortion Through 70 Days' Gestation
|
N/A | |
Suspended |
NCT03751423 -
Intravenous Ketamine for Pain Control During First Trimester Surgical Abortion
|
Phase 3 | |
Completed |
NCT03480009 -
Dextromethorphan as a Novel Non-opioid Adjunctive Agent for Pain Control in Medication Abortion
|
Phase 3 | |
Completed |
NCT05469594 -
Second-trimester TOP : a Retrospective Study Comparing Complications at 12-14 vs 14-16 Weeks of Gestation
|
||
Completed |
NCT05320432 -
Transcutaneous Electrical Nerve Stimulation for Pain Control During First-trimester Abortion
|
N/A | |
Completed |
NCT03187002 -
Transcutaneous Electrical Nerve Stimulation (TENS) for Pain Control During First Trimester Abortion
|
N/A | |
Terminated |
NCT04139382 -
Using Telemedicine to Improve Early Medical Abortion at Home
|
N/A | |
Recruiting |
NCT04956731 -
Pharmacist Provision of Medication Abortion
|
N/A | |
Recruiting |
NCT04336358 -
Telemedicine for First Trimester Abortion in South Africa
|
N/A | |
Completed |
NCT02096575 -
Nitrous Oxide for Pain Management of First Trimester Surgical Abortion
|
N/A |