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Efficacy of Sublingual administration Misoprostol 600 mcg versus 800 mcg for induced abortion in women with early pregnancy loss: A Randomized Controlled Trial

Efficacy of Sublingual administration Misoprostol 600 mcg versus 800 mcg for induced abortion in women with early pregnancy loss: A Randomized Controlled Trial

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
TCTR
Registry ID
TCTR20210303009
Enrollment
108
Registered
2021-03-03
Start date
2020-04-10
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pregnant women which gestational age less than 12 weeks with early pregnancy loss. Early pregnancy loss Medical abortion Misoprostol

Interventions

600 mcg misoprostol sublingually administrated every 6 hours maximum 3 doses,800 mcg misoprostol sublingually administrated every 6 hours maximum 3 doses
600 mcg misoprosto,800 mcg misoprostol

Sponsors

No
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 18-year-old pregnant women who were below 12 weeks of gestational age and diagnosed with an early pregnancy loss with stable vital signs, closed internal cervical os, no contraindication for misoprostol, no active bleeding, no abnormal pregnancy (ectopic pregnancy, molar pregnancy) were included

Exclusion criteria

Exclusion criteria: Women who were not able to follow up were excluded from this study.

Design outcomes

Primary

MeasureTime frame
success rate within 7 days Transvaginal ultrasound after 7 days of administration of misoprostol

Secondary

MeasureTime frame
success rate within 7 days within 7 days after administration misoprostol, if ET less than 10mm defined as complete abortion which is success rate

Countries

Thailand

Contacts

Public ContactBenjamas Klunkaew

Queen Savang Vadhana Memorial Hospital

roseapplechomp@gmail.com0809072062

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026