Efficacy of pain relief during first trimester surgical abortion : randomized clinical trial compared intravenous sedation, paracervical block and lidocaine spray added to paracervical block
Phase 4
Recruiting
- Conditions
- incomplete abortion
- Registration Number
- TCTR20180802002
- Lead Sponsor
- sanpasitthiprasong hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 165
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
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method pain score during procedure after received intervention numerical rating scale
- Secondary Outcome Measures
Name Time Method side effect of drugs, satisfactory to procedure, additional analgesic used 30 minutes after procedure Questionnaire interview