Intrauterine Lidocaine versus Placebo in Conjunction with Paracervical Block for Pain Relief During Fractional Curettage: A Randomized Controlled Trial

Phase 3

Recruiting

• Conditions: Anaesthesiology - Anaesthetics; Adverse effects in women with abnormal uterine bleeding who undergoing fractional and curettage; Pain score in women with abnormal uterine bleeding who undergoing fractional and curettage; Additional drug requirement in women with abnormal uterine bleeding who undergoing fractional and curettage

• Registration Number: ACTRN12611000449932
• Lead Sponsor: Khon Kaen Hospital

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2011-05-03
• Last Update Posted: 13 January 2020

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 230

Inclusion Criteria

Women with abnormal uterine bleeding who undergoing fractional and curettage

Exclusion Criteria

Pregnancy
Hx of lidocaine hypersensitivity
Hx of bleeding disorders
Hx of impaired LFT
Taking anti-coagulants
Genital organ infection
Profuse uterine bleeding or vital signs unstable

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain score[After speculum insertion, During and immediately after the procedure]

Secondary Outcome Measures

Name	Time	Method
Adverse effects e.g. dizziness, nausea and/or vomiting, postural hypotension, convulsion. These adverse effects will be assessed using questionnaire by nurse who does not involve in the previous procedure.[During, immediately, and until 2 hour after the procedure];Additional drug requirement will be assessed by medical record ('yes' or 'no')[During the procedure]