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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT00750906
Other study ID # H898-32701
Secondary ID
Status Terminated
Phase
First received
Last updated
Start date October 2008
Est. completion date April 30, 2015

Study information

Verified date January 2020
Source University of California, San Francisco
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study will be conducted to determine the pharmacodynamics, cardiovascular and biochemical effects of succinylcholine when given during electroconvulsive therapy. (ECT). This is a single center, prospective, study in patients who will be receiving ECT as indicated and prescribed by their psychiatrist. The study will be performed twice on each patient, 48-72 hours apart during consecutively scheduled ECT procedures.


Description:

Patients will receive the anesthetic that is traditionally given which includes appropriate doses of succinylcholine. Serum potassium and creatinine phosphokinase (CK) levels will be determined pre and post anesthesia; serum and urine myoglobin will be determined post anesthesia. Vital signs data [i.e., heart rate (arrhythmias) and arterial blood pressure] will be compared pre and post anesthesia. In addition patients will be asked about the presence of muscle pain (myalgia) 1 hour before discharge from the recovery room and the following day post ECT.


Recruitment information / eligibility

Status Terminated
Enrollment 13
Est. completion date April 30, 2015
Est. primary completion date April 30, 2015
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

1. A male or non-pregnant female aged 18 years and older

2. American Society of Anesthesiologists physical status 1, 2, 3

3. Scheduled to undergo electroconvulsive therapy under general anesthesia

4. Have given written informed consent

Exclusion Criteria:

1. Pregnant or nursing

2. Any patient in the study investigators opinion who may not be suitable for research.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
United States University of California San Francisco San Francisco California

Sponsors (1)

Lead Sponsor Collaborator
University of California, San Francisco

Country where clinical trial is conducted

United States, 

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