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
Completed
- Conditions
- Surgeryocal anesthesia for fractional curettageFractional curettage
- Registration Number
- ISRCTN02384619
- Lead Sponsor
- Mahidol University - Siriraj Grant for Research Development (Thailand)
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Female
- Target Recruitment
- 70
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.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The reduction of a maximum pain score during fractional curettage.
- Secondary Outcome Measures
Name Time Method Secondary outcomes included pain profile during fractional curettage, number of patients with pain score >4 cm, patients? global satisfaction, types and incidence of adverse events, and serum lidocaine profile.