aropin vs. Marcaine in Pudendal Nerve Block in Open Haemorroidectomy

Phase 4

Withdrawn

• Conditions: Open haemorrhoidectomy; Surgery - Surgical techniques; Anaesthesiology - Anaesthetics

• Registration Number: ACTRN12612000126819
• Lead Sponsor: Gold Coast Hospital

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2012-01-25
• Last Update Posted: 13 January 2020

Recruitment & Eligibility

• Status: Withdrawn
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

All adult participants who have haemorrhoids and require surgery.

Exclusion Criteria

Allergic to either local anaesthetic agents or refuse to participate in the study.
Pregnancy: no unnecessary general anaesthetic
Children/young people: can't consent to study, and also their prticipation in answering the questionnaire maybe subjectively inadequate.
people highly dependent on medical care: inadequate consent and unable to participate in the questionnaire.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
To compare the effectivness between two local anaesthetic agents in performing Pudendal nerve block[Assessed daily for the first 7 days then at a 2 weeks.<br>Assessments will be a preoperative questionaire and postoperative questionaire regarding expected level of pain and postoperative pain score and use of oral analgesics.]

Secondary Outcome Measures

Name	Time	Method
Evaluate the amount of oral analgesics used and to compare that to the type of the local anaesthetic used.[Assessed daily for the first 7 days then at a 2 weeks.<br>Assessments will be a preoperative questionaire and postoperative questionaire regarding expected level of pain and postoperative pain score and use of oral analgesics.];Participation of Sitz Bath ( Salt bath) manoeuvre in relief of pain. This is not compulsory the use of one will just be captured.[Assessed daily for the first 7 days then at a 2 weeks.<br>Assessments will be a preoperative questionaire and postoperative questionaire regarding expected level of pain and postoperative pain score and use of oral analgesics.]