Bolus Dosing of Remifentanil with Propofol for Gynaecological Day Case Surgery

Not Applicable

Completed

• Conditions: Surgery: Anaesthesia; Surgery

• Registration Number: ISRCTN27187868
• Lead Sponsor: Department of Health

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2004-09-30
• Study Completion: 2005-07-13
• Last Update Posted: 24 August 2021

Recruitment & Eligibility

• Status: Completed
• Sex: Female
• Target Recruitment: 0

Inclusion Criteria

ASA 1 and 2 subjects presenting for routine elective minor gynaecological day case surgery. All patients attending for surgery will be given a patient information leaflet and those agreeing to participate in the study will be asked to sign a consent form. They will be the subject of therapeutic research.

Exclusion Criteria

Patients giving history of reflux or hiatus hernia, obesity or cases requiring tracheal intubation for any other reason.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<br> 1. Time from end of procedure to<br> 1.1. eyes open<br> 1.2. recollection of name<br> 1.3. fitness to discharge from recovery<br> 1.4. ready for home discharge<br> 2. post-operative pain<br> 3. analgesic requirements<br> 4. nausea and vomiting<br> 5. total dose of agents used<br>

Secondary Outcome Measures

Name	Time	Method
ot provided at time of registration