Effect of General Anesthetic Dose on Recovery From Surgery Clinical Trial
Official title:
The BALANCED Anaesthesia Study A Prospective, Randomised Clinical Trial of Two Levels of Anaesthetic Depth on Patient Outcome After Major Surgery
| NCT number | NCT02073357 |
| Other study ID # | 13-1195 |
| Secondary ID | |
| Status | Withdrawn |
| Phase | N/A |
| First received | February 25, 2014 |
| Last updated | July 29, 2014 |
| Start date | July 2014 |
General anaesthesia is a reversible drug-induced coma. Too little can result in patients
being partially conscious during surgery; too much can slow recovery after surgery. There is
a range of drug doses that can be used and some anesthesiologists use more than others.
There is no convincing evidence that any particular dose within the usual range is better.
Consequently, there are no guidelines on the best depth of anaesthesia. This study will
determine whether general anesthetic concentrations at the low end of the usual range are
better than those at the high end.
Participants will randomly be assigned to lighter or deeper general anesthesia. The first
day after surgery, two short questionnaires about recovery and memories of the surgery will
be completed. During the rest of the participant's hospital stay, a survey about how one
feels will be completed.
There will be two telephone contacts after discharge from the hospital. One month after
surgery three questionnaires will be completed about performing daily tasks, how you feel
and memories of the surgery. Then one year after surgery pain will be assessed.
| Status | Withdrawn |
| Enrollment | 0 |
| Est. completion date | |
| Est. primary completion date | January 2019 |
| Accepts healthy volunteers | No |
| Gender | Both |
| Age group | 60 Years and older |
| Eligibility |
Inclusion Criteria: - Age =60 years - ASA physical status 3 or 4 - surgery expected to last =2 hours - post-operative hospital stay expected to be =2 nights - general anaesthesia with or without major regional block - able to monitor BIS throughout anaesthesia Exclusion Criteria: - Unable to monitor BIS (e.g. cranial or intracranial surgery) - unable to consent - surgery with 'wake-up' test - propofol infusion for part or all of maintenance of anaesthesia ('total intravenous anaesthesia') - previous enrolment in Balanced study |
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor), Primary Purpose: Treatment
| Country | Name | City | State |
|---|---|---|---|
| United States | Cleveland Clinic | Cleveland | Ohio |
| Lead Sponsor | Collaborator |
|---|---|
| The Cleveland Clinic | National Health and Medical Research Council, Australia |
United States,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | One-year all-cause mortality | One year | Yes |