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Clinical Trials/ChiCTR-OOC-16008511
ChiCTR-OOC-16008511RecruitingUnknown

手動式真空吸引術、保守治療、外科手術及單次陰道塞劑(misoprostol)對早孕期流產之婦女的生理及心理之影響

Not provided1 site in 1 country100 target enrollmentStarted: January 1, 1990Last updated:

Trial Snapshot

Phase
Unknown
Status
Recruiting
Enrollment
100
Locations
1
Primary Endpoint
1. To assess the complete miscarriage rates and its complications of each treatment modalities

Study Overview

Brief Summary

手動式真空吸引術、保守治療、外科手術及單次陰道塞劑(misoprostol)對早孕期流產之婦女的生理及心理之影響

Study Design

Study Type
Observational

Eligibility Criteria

Ages
18 to 50 (—)
Sex
Female

Inclusion Criteria

  • Women who present with spontaneous miscarriage.

Exclusion Criteria

  • severe blood loss;
  • clinically presenting sepsis;
  • patient refusal.

Arms & Interventions

Case series

NA, This study only require participants to fill in questionnaires

Outcomes

Primary Outcomes

1. To assess the complete miscarriage rates and its complications of each treatment modalities

Time Frame: observe clinical outcome at the day of admission and 7 days, 14 days, 28 days and 6 months after miscarriage

Secondary Outcomes

  • 3. To assess the psychological outcomes of currently acceptable forms of treatment, with a focus the miscarrying woman’s experience(at the day of admission and 7 days, 14 days, 28 days and 6 months after miscarriage)

Investigators

Sponsor
Not provided

Study Sites (1)

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手動式真空吸引術、保守治療、外科手術及單次陰道塞劑(misoprostol)對早孕期流... | Clinical Trial