CompletedNot Applicable

Treatment of Incomplete Abortion With 600 Mcg Oral Misoprostol Compared to Standard Surgical Treatment

Ecuador, Venezuela311 participantsStarted 2006-05

Plain-language summary

This study aims to compare the efficacy, side effects profile and acceptability of a single dose of 600mcg misoprostol taken orally compared to standard surgical treatment as per local protocols for the treatment of incomplete abortion.

Who can participate

Age range

14 Years

Sex

FEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * past or present history of vaginal bleeding during pregnancy * open cervical os * evidence of incomplete abortion with substantial debris in the uterus (if using ultrasound) * surgical evacuation of the uterus would be advised as course of action if misoprostol was not available * generally in good health * woman lives or works within one hour of study site * woman willing to provide contact information for follow up purposes * informed consent given Exclusion Criteria: * contraindications to study drug * uterine size larger than 12 weeks LMP * signs of severe infection

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

complete resolution of signs/symptoms of incomplete abortion without recourse to surgery at any point for any reason

Timeframe: one week after initial treatment

Trial details

NCT IDNCT00674232

SponsorGynuity Health Projects

Sponsor typeOTHER

Study typeINTERVENTIONAL

View on ClinicalTrials.gov More Incomplete Abortion trials