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Clinical Trials/ISRCTN02384619
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.

Registry
who.int
Start Date
July 8, 2005
End Date
TBD
Last Updated
11 years ago
Study Type
Interventional
Sex
Female

Investigators

Sponsor
Mahidol University - Siriraj Grant for Research Development (Thailand)

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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