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Evaluating the effectiveness of ketamine on muscle pain (myalgia), headache and restlessness (agitation) after electroconvulsive therapy in patients with major depression disorder.

Survey the effectiveness of ketamine on myalgia, headache and agitation in Major Depression patients after electroconvulsive therapy.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT138904221766N4
Enrollment
50
Registered
2011-11-19
Start date
2011-10-16
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Electroconvoulsive therapy induced myalgia. Myalgia

Interventions

Intervention 1: Control group: In this group 2 ml normal saline (placebo) will be injected before any other drugs in zero time. Intervention 2: Study group: In this group 30 Mg Ketamine that had been
Prevention
Control group: In this group 2 ml normal saline (placebo) will be injected before any other drugs in zero time.
Study group: In this group 30 Mg Ketamine that had been diluted in 2 ml normal saline will be injected before any other drugs in zero time.

Sponsors

Kurdistan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Major depression based on DSM 4 criteria, physical condition in accordance with ASA Class 1 or 2, ability and capacity to sign informed consent sheet. Exclusion criteria: history of major systemic disease, history of neuromuscular disease, history of myalgia.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Myalgia. Timepoint: At 6, 12, 24 and 48 hours after ECT. Method of measurement: Myalgia graded as follow: absence of myalgia = no; stiffness or muscle pain did not need treatment = mild; muscle pain or stiffness reported spontaneously by the patient, and required therapy = moderate; very severe discomfort = severe.;Headache. Timepoint: In the first 24 hours after ECT. Method of measurement: Visual Analoge Scale.;Agitation. Timepoint: In the recovery period. Method of measurement: 1. Yes: motor restlessness, severe motor movement, and besides, un-aimed try to leave the bed, wanting to get up from bed, high loud crying, pulling catheters, confusion and poor response to verbal commands) 2 . No: not mentioned in any of the above scenarios.

Secondary

MeasureTime frame
Seizure duration. Timepoint: After induction of ECT. Method of measurement: Second.;Mean arteial blood preasure. Timepoint: Befor induction of anesthesia ,after induction of anesthesia ,and after termination of seizure. Method of measurement: Milimeter of Hg.;Heart Rate. Timepoint: Befor induction of anesthesia , after induction of anesthesia ,and after termination of seizure. Method of measurement: Beat /minute.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactZohreh Ziaee

Faculty of Medicine

dr.ziaee24@yahoo.com+98 87 1666 4664

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026