ISRCTN02384619
Completed
Not Applicable
A double blind randomised placebo-controlled trial to compare the effectiveness of paracervical block plus Intrauterine anesthesia and paracervical block alone for pain relief during fractional durettage
Mahidol University - Siriraj Grant for Research Development (Thailand)0 sites70 target enrollmentJuly 8, 2005
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- ocal anesthesia for fractional curettage
- Sponsor
- Mahidol University - Siriraj Grant for Research Development (Thailand)
- Enrollment
- 70
- Status
- Completed
- Last Updated
- 11 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Women with abnormal uterine bleeding scheduled for fractional curettage.
Exclusion Criteria
- •Patients who had the American Society of Anesthesiologists (ASA) physical status \>II, genital organ infection, profuse uterine bleeding, a history of lidocaine hypersensitivity, a history of impaired liver function, were virgin, pregnant, or unable to understand how to score a 10\-cm visual analogue scale (VAS) pain score.
Outcomes
Primary Outcomes
Not specified
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