Abortion in First Trimester Clinical Trial
Official title:
Auriculotherapy as an Adjunct for Pain Management During First Trimester Vacuum Aspiration Abortion: a Randomized, Double-blinded, Three Arm Trial
Verified date | February 2021 |
Source | Columbia University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Primary Objective: To assess whether usual care plus auricular acupressure with beads reduces subject-reported maximum pain during first trimester vacuum aspiration compared to usual care plus placebo. Secondary Objective: To assess whether usual care plus auricular acupuncture with Pyonex™ needles reduces subject-reported maximum pain during first trimester vacuum aspiration as compared to usual care plus placebo. This assessment will replicate the previous trial and strengthen the evidence that auricular acupuncture is beneficial for aspiration abortion pain Exploratory Objective: To assess whether usual care plus either auricular acupressure with beads or auricular acupuncture with Pyonex™ needles reduces subject-reported anxiety scores during first trimester vacuum aspiration as compared to women receiving usual care plus placebo.
Status | Completed |
Enrollment | 177 |
Est. completion date | December 12, 2019 |
Est. primary completion date | December 12, 2019 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 18 Years and older |
Eligibility | bullets Inclusion Criteria: - Pregnant up to 13 weeks gestation - Seeking aspiration abortion for any first trimester induced abortion, abnormal pregnancy, early pregnancy loss, retained products of conception, or molar pregnancy - English- or Spanish-speaking - Willingness to be randomized into one of the three arms. Exclusion Criteria: - Allergy to adhesives or gold - Allergy or intolerance to ibuprofen or 1% lidocaine (paracervical block) - Congenital anomaly or infection of the ear. |
Country | Name | City | State |
---|---|---|---|
United States | Columbia University Medical Center | New York | New York |
Lead Sponsor | Collaborator |
---|---|
Columbia University | Society of Family Planning |
United States,
Ndubisi C, Danvers A, Gold MA, Morrow L, Westhoff CL. Auricular acupuncture as an adjunct for pain management during first trimester abortion: a randomized, double-blinded, three arm trial. Contraception. 2019 Mar;99(3):143-147. doi: 10.1016/j.contraception.2018.11.016. Epub 2018 Dec 7. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Anxiety Visual Analog Scale Score | Self-assessed maximum anxiety reported using a 0-100 mm visual analog scale, where 100 signifies maximum anxiety. To measure anxiety during aspiration abortion. | Immediately following the aspiration abortion procedure (approximately 10 minutes) | |
Primary | Pain Visual Analog Scale Score (Beads vs Placebo) | Self-assessed maximum pain reported using a 0-100mm visual analog scale, where 100 signifies maximum pain. To measure pain experienced during aspiration abortion. | Immediately following the aspiration abortion procedure (approximately 10 minutes) | |
Secondary | Pain Visual Analog Scale Score (Needles vs Placebo) | Self-assessed maximum pain reported using a 0-100mm visual analog scale, where 100 signifies maximum pain. To measure pain experienced during aspiration abortion. | Immediately following the aspiration abortion procedure (approximately 10 minutes) |
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 | |
Completed |
NCT03079622 -
Manual Versus Electric Vacuum Aspiration for Pregnancy Termination Between 10-14 Weeks
|
N/A | |
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 |
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 |