TCTR20180802002RecruitingPhase 4
Efficacy of pain relief during first trimester surgical abortion : randomized clinical trial compared intravenous sedation, paracervical block and lidocaine spray added to paracervical block
Conditions
Trial Snapshot
- Phase
- Phase 4
- Status
- Recruiting
- Sponsor
- sanpasitthiprasong hospital
- Enrollment
- 165
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
- Ages
- 15 Years to 45 Years (—)
- Sex
- Female
Inclusion Criteria
- •pregnant woman with gestational age below 14 weeks who diagnosed incomplete abortion
Exclusion Criteria
- •- allergy to meperidine or lidocaine
- •- septic abortion
- •- unstable vital signs
- •- patients who can not communicate and unconscious
Investigators
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