NCT02394847

Brief Summary

Electroconvulsive therapy has been used for many years for different types of physiatric diseases. General anesthesia is used during the procedure. Different anesthesiologists use different regimens. The duration of seizure is important in this procedure. The investigators evaluated the relationship between the dose of propofol and the number of electroconvulsive therapy and duration of the seizure.

Trial Health

100
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
10

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Jan 2012

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2012

Completed
11 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2012

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2012

Completed
2.3 years until next milestone

First Submitted

Initial submission to the registry

March 8, 2015

Completed
12 days until next milestone

First Posted

Study publicly available on registry

March 20, 2015

Completed
Last Updated

March 20, 2015

Status Verified

March 1, 2015

Enrollment Period

11 months

First QC Date

March 8, 2015

Last Update Submit

March 17, 2015

Conditions

Keywords

propofolelectroconvulsive therapyanesthesia

Outcome Measures

Primary Outcomes (1)

  • dose of propofol

    10 seconds

Secondary Outcomes (1)

  • duration of seizure

    10 seconds

Study Arms (1)

propofol

OTHER

dose of propofol according to the number of therapies

Drug: propofol

Interventions

propofol

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Patients required electroconvulsive therapy for the physiatric disease

You may not qualify if:

  • Patients refusal

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Interventions

Propofol

Intervention Hierarchy (Ancestors)

PhenolsBenzene DerivativesHydrocarbons, AromaticHydrocarbons, CyclicHydrocarbonsOrganic Chemicals

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
SCREENING
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
specialist anesthesiologist

Study Record Dates

First Submitted

March 8, 2015

First Posted

March 20, 2015

Study Start

January 1, 2012

Primary Completion

December 1, 2012

Study Completion

December 1, 2012

Last Updated

March 20, 2015

Record last verified: 2015-03