MAPD: Modifiable Factors Affecting Propofol Dosing

CompletedOBSERVATIONAL
Enrollment

91

Participants

Timeline

Start Date

April 1, 2018

Primary Completion Date

December 1, 2018

Study Completion Date

August 31, 2019

Conditions
Anesthesia
Interventions
OTHER

Preoperative Questionnaires

"The participants will be asked to complete 5 questionnaires:~1. An abbreviated version of the Caffeine Assessment Tool (CAT)~2. Sleep Questionnaire (SQ)~3. Surgical Fear Questionnaire (SFQ)~4. WHO Alcohol AUDIT Tool~5. WHO Smoking Questionnaire~They will also be asked to complete a demographics sheet~All participants will undergo standard anaesthetic induction, a research participant will observe the dose of propofol and time taken for loss of consciousness"

OTHER

Postoperative Subjective Pain Scores

After the operation, participants will be provide with a scale from 1-10 in which to rate their pain at rest and whilst coughing. This will be undertaken at 1hr postoperatively.

Trial Locations (1)

SW109NH

Chelsea and Westminster Hospital, London

All Listed Sponsors
lead

Chelsea and Westminster NHS Foundation Trust

OTHER

NCT03453099 - MAPD: Modifiable Factors Affecting Propofol Dosing | Biotech Hunter | Biotech Hunter