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The Physical and Psychological Outcomes of Expectant Management, Surgical Evacuation or Medical Evacuation with Single Dose 800 mcg Vaginal Misoprostol for Women with First Trimester Miscarriage in a Randomized Controlled Trial

The Physical and Psychological Outcomes of Expectant Management, Surgical Evacuation or Medical Evacuation with Single Dose 800 mcg Vaginal Misoprostol for Women with First Trimester Miscarriage in a Randomized Controlled Trial

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-08000725
Enrollment
Unknown
Registered
2008-08-28
Start date
2008-09-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

trimester miscarriage

Interventions

Two groups:Expectant management, Surgical evacuation or Medical evacuation with single dose 800 mcg Misoprostol for two weeks versus Expectant management, Surgical evacuation or Medical evacuation wit

Sponsors

None listed

Eligibility

Sex/Gender
Male
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. To be aged older than 18 years old HK citizen; 2. Good past health; 3. Gestation age less than 13 weeks; 4. Ultrasound confirmed the diagnosis of miscarriage: (a) intrauterine gestational sac with mean sac diameter of >=2cm without fetal pole; (b) presence of fetal pole with no cardiac pulsation; (c) the gestational sac was <2cm with no interval growth or persistent absence of fetal cardiac pulsation on rescanning 7 to 10 days later. 5. Incomplete miscarriage which is supported by opened endocervical os and ultrasound findings of an endometrial echo showing mixed echogenicity.

Exclusion criteria

Exclusion criteria: 1. Women had complete miscarriage which was supported by an intrauterine dimension measuring <11cm2 (sagittal plus transverse plane) on ultrasound; 2. Severe blood loss, sepsis; 3. Known allergy to prostaglandin or their analogues; 4. Any reason that the attending clinician thinks that may make the patient unsuitable for misoprostol administration.

Design outcomes

Primary

MeasureTime frame
1. To assess the complete miscarriage rates and its complications of each treatment modalities;2. To determine the predictive factors for successful outcome of currently acceptable forms of treatment;3. To assess the acceptance and satisfaction of treatment;4. To assess the psychological outcomes of currently acceptable forms of treatment, with a focus the miscarrying woman's experience;5. To assess the women's preference of currently acceptable forms of treatment;6. To assess the psychological impact of father of pregnancy during treatment;

Countries

China

Contacts

Public ContactKong Wing Shan Grace
gracekong@cuhk.edu.hk+852 26322996

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026