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Effect of Hyoscine and Atropine on blood pressure ,heart rate in patient who treated by ECT

Comparisson of the effect of pretreatment with Hyoscine,Atropine and placebo on hemodynamic stability,recovery time,and ECT side effect

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014100719431N1
Enrollment
60
Registered
2015-01-12
Start date
2014-03-20
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

Condition 1: Schizophrenia. Condition 2: Persistant delusional disorders. Condition 3: Acute and transient psychotic disorder. Condition 4: Manic disorder. Condition 5: Bipolar mood diorder. Condition 6: Depressive episode. Condition 7: Paranoid personality disorder. Schizophrenia Persistant delusional disorder Acute and transient psychotic disorder Manic episode Bipolar affective disorder Depressive episode Paranoid personality disorder

Interventions

Intervention 1: 20 patients accidentally are belong to first group.after initial monitoring and record of information,vital signs include systolic and diastolic blood pressure,pulse rate are recorded
Treatment - Drugs
20 patients accidentally are belong to first group.after initial monitoring and record of information,vital signs include systolic and diastolic blood pressure,pulse rate are recorded in data sheath.i
20 patients accidentally are belong to second group.after initial monitoring and record of information,vital signs include systolic and diastolic blood pressure,pulse rate are recorded in data sheath.
20 patients accidentally are belong to third group.after initial monitoring and record of information,vital signs include systolic and diastolic blood pressure,pulse rate are recorded in data sheath.i

Sponsors

Iran University of Medical Science
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 70 Years

Inclusion criteria

Inclusion criteria: patients according to psychological indication and psychologist confirmation are entered to study patients excep who are older than 70 and those have medical contraindication for atropine and hyoscine. patients have tachy cardia,bradycardia,arrythmia,hypotension and hypertension are excluded.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Heart rate. Timepoint: after and before pretreatment and after induction and immediately ,after 1,3 and 5 minutes from shock ,heart rate is measured in all patients. Method of measurement: heart rate is measuring by ECG monitoring.;Duration of convulsion. Timepoint: after shock,from the firs movements of patientsto end of convulsion,time is recorded. Method of measurement: duration of convulsion is measured according to seconds.;Time of recovery. Timepoint: from termination of convulsion to allertness of patient is called as recovery time.alertness means the ability of patients to obey orders. Method of measurement: time of recovery,allertness and obey is measuring according minutes.;Volume of respiratory secretions. Timepoint: by convulsion termination ,respiratory secretions may ecceed normal amounts ,so we should suction them. Method of measurement: volume of secretions is measured according to how many times to sucction(1-3 times )1:dry 2:sialorrhea 3:huge amounts of secretions.;Blood pressure. Timepoint: after and before pretreatment and after induction and immediately ,after 1,3 and 5 minutes from shock ,blood pressure is measured in all patients. Method of measurement: blood pressure is measured by cuff around patients arm.

Secondary

MeasureTime frame
Cognition disorders. Timepoint: cognition disorders are recorded during recovery time. Method of measurement: cognition disorders according to diagnosis confirmation by psychologist.;Other complications. Timepoint: from the patients entrance to end of recovery. Method of measurement: every other complication occurs is recorded by inspection and visualization.;Primary diagnosis. Timepoint: at first after patients entrance, primary diagnosis is recorded in data sheet. Method of measurement: at first primary diagnosis is recorded from medical records.;Age. Timepoint: at first after patients entrance, age is recorded. Method of measurement: age is recorded according to medical records.;Sex. Timepoint: at first,after patients entrance, sex is recorded. Method of measurement: at first sex is recorded from medical records.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactBehnaz Karimi

Iran University of Medical Science

karimi.behnaz@gmail.com+98 21 4476 3217

Outcome results

None listed

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