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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04316325
Other study ID # POC-OPT-1902-31934
Secondary ID
Status Completed
Phase
First received
Last updated
Start date March 20, 2020
Est. completion date March 31, 2021

Study information

Verified date September 2021
Source Reproductive Health Training Center of the Republic of Moldova
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study evaluates the safety, feasibility, and acceptability of a novel medical abortion via telemedicine service in the Republic of Moldova.


Description:

Women and girls in Moldova, especially those in rural areas, must travel to regional medical centers to obtain an abortion from a certified gynecologist. This creates barriers to accessing safe abortion that disproportionately affect poor women and girls, through wage loss due to missed work and accrued costs due to transportation. This innovation is a novel service delivery model that allows self-management of medical abortion (MA) with remote guidance from a provider. After confirming their pregnancy, women seeking MA will receive counseling from a gynecologist via videoconference and will subsequently obtain the necessary medication via mail or at at participating pharmacy with prescription. Follow-up will occur 1 weeks later via phone/videoconference (with referral to a doctor if necessary) to confirm MA success and assess the patient's and provider's satisfaction with the service. We hope to demonstrate the feasibility, effectiveness and acceptability of telemedicine MA services in Moldova so that it can thus be integrated into the national public healthcare system. As a result, this project will serve as a model that could be adapted and implemented in nearby countries within the Eastern Europe and Central Asia region.


Recruitment information / eligibility

Status Completed
Enrollment 549
Est. completion date March 31, 2021
Est. primary completion date March 31, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 16 Years and older
Eligibility Inclusion Criteria: - 16 years or older - Has an unwanted pregnancy - Confirmed the pregnancy using a test or via ultrasound - Gestational age of 9 weeks or less - Has personally decided to end the pregnancy - Has a device (phone, tablet, or computer) with internet connection, a webcam, and a microphone. - Has immediate access to emergency services - Reports no contraindication to medical abortion Exclusion Criteria: - Under 16 years of age - Does not have an unwanted pregnancy - Did not confirm pregnancy - Gestational age greater than 9 weeks - Does not have a device (phone, tablet, or computer) with internet connection, a webcam, and a microphone - Does not have immediate access to emergency services - Has an intrauterine device - Is allergic to abortion medications (mifepristone or misoprostol) - Has severe anemia or acute porphyria - Has a condition that affects the ability of blood to clot normally - Has hepatic failure or chronic renal disease - Has an ectopic pregnancy - Has heart disease or other cardiovascular problem - Has a condition that requires hormone treatment

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Medical abortion
Trained abortion providers will counsel participants about medical abortion via videoconference or telephone, the abortion medications will be sent to the participants via mail or will be accessed at a pharmacy, the provider will follow up one week later with the participants to assess outcomes, and four weeks later the participant will take a pregnancy test to confirm completion of the abortion

Locations

Country Name City State
Moldova, Republic of Reproductive Health Training Center Chisinau

Sponsors (3)

Lead Sponsor Collaborator
Reproductive Health Training Center of the Republic of Moldova Grand Challenges Canada, Gynuity Health Projects

Country where clinical trial is conducted

Moldova, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Successful termination of pregnancy without adverse events Percentage of study participants that successfully terminate their pregnancy via the telemedicine medical abortion model without experiencing any adverse events. through study completion, around 15 months
Secondary Participant satisfaction with the medical abortion via telemedicine service Percentage of study participants that report being satisfied or very satisfied with the medical abortion via telemedicine service. through study completion, around 15 months
Secondary Cost savings experienced by study participants Percentage cost savings among study participants receiving medical abortion via telemedicine in comparison with the cost of in-person medical abortion. through study completion, around 15 months
Secondary Provider satisfaction Percentage of medical abortion providers that report being satisfied or very satisfied with the telemedicine service provision process. through study completion, around 15 months
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