AzTrials
AzTrials

Major Depressive DisorderPhase 4ECaTaNCT04828226

Clonidine to Prevent Delirium After Electroconvulsive Therapy.

A Phase 4 study testing Clonidine in people with Major Depressive Disorder and Catatonia, run by Insel Gruppe AG, University Hospital Bern at 1 site in Switzerland.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
Search all trials

Trial summary

Electroconvulsive therapy (ECT) is a highly effective treatment for some psychiatric disorders like major depressive or bipolar disorder, but may lead to agitation and delirium after the procedure in up to 65% of patients. This can have negative side effects and be dangerous for patient and attending staff. Read more about this study

Who is it for?
Ages 18 years and older
What is being tested?
Clonidine
Type of treatment
Injection or infusion
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
130 participants
Where
1 siteSwitzerland
Study dates
27 Apr 2021to 16 May 2026
Phase
Phase 4
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Aged 18 and more;
  • Scheduled for an elective series of ambulatory ECT sessions at the University Hospital Bern;
  • Informed Consent as documented by signature (Appendix Informed Consent Form).

Who cannot join

  • Contraindications to the study drug, e. g. known allergy or hypersensitivity, hypotension, bradycardia, higher grade atrioventricular block;
  • On regular Clonidine for another indication (e.g. arterial hypertension)
  • Patients undergoing emergency ECT;
  • Unable to consent (incapable of judgment, next-of-kin consent necessary or under tutelage);
  • Inability to follow the procedures of the study, e. g. due to language barrier;
  • Previous enrolment into the current study;
Show all 11Show fewer
  • Participation in another study with investigational drug within the 30 days preceding and during the present study;
  • Enrolment of the investigator, his/her family members, employees and other dependent persons.
  • Women who are pregnant or breast feeding;
  • Intention to become pregnant during the course of the study;
  • Lack of safe contraception, defined as: Female participants of childbearing potential, not using and not willing to continue using a medically reliable method of contraception for the entire study duration (and 4 weeks thereafter), such as oral, injectable, or implantable contraceptives, or intrauterine contraceptive devices, or who are not using any other method considered sufficiently reliable by the investigator in individual cases. Female participants who are surgically sterilised / hysterectomised or post-menopausal for longer than 2 years are not considered as being of child bearing potential.

Trial locations and contacts

1 site in 1 country.

Switzerland1 site
  • Department of Anaesthesiology and Pain Medicine, Bern University Hospital, University of Bern

    Bern, 3010

Other trials in Switzerland

About this study

Official title: Clonidine to Prevent Postictal Delirium After ElectroConvulsive Therapy: a Randomised, Placebo-controlled, Triple-blind, Single-centre Trial.

Electroconvulsive therapy (ECT) is a highly effective treatment for some psychiatric disorders like major depressive or bipolar disorder, but may lead to agitation and delirium after the procedure in up to 65% of patients. This can have negative side effects and be dangerous for patient and attending staff. Clonidine, a central-acting alpha2-receptor agonist, is an approved antihypertensive medication with known sedative side effects. Clonidine's newer but more expensive successor, dexmedetomidine, has recently shown its potential to reduce this kind of delirium. The investigators therefore hypothesise that pre-treatment with 2 mcg/kg clonidine prior to electroconvulsive therapy will significantly reduce the incidence of postictal delirium. This potentially makes a highly efficient treatment for patients with otherwise refractory psychiatric illness safer and more accessible.

Read the detailed description

Electroconvulsive therapy (ECT) is a highly efficacious therapy for psychiatric disorders, especially major depressive disorder, bipolar disorder and catatonia resistant to psychopharmacology or drug-psychotherapy combination therapy. At therapy induction, usually a series of 10-12 ECT sessions is planned with two to three days in between sessions. Thereafter, maintenance therapy can be continued with longer session intervals thereafter to avoid relapses and to support further drug and psychotherapy treatment. Without maintenance therapy, relapses can happen in up to 80% of all patients within one year.

Nowadays conducted under general anaesthesia (etomidate in the investigator's centre) and muscle relaxation (suxamethonium) to prevent adverse events, ECT can be challenging for the anaesthesiologist, as it usually leads to rapid cardiovascular changes such as sudden bradycardia due to vagal discharge, followed by sympathetic counter regulation associated with tachycardia and hypertension. For the patient, known immediate side effects are headache in about 30% and postictal confusion and delirium in up to 65%. This confusional state can lead to involuntary movements and agitation and therefore be harmful for patients and attending staff. It usually resolves within 45 minutes but nevertheless seems to be linked with adverse side effects like persistent retrograde amnesia. Identified risk factors are long seizure time and pre-existing catatonic features. Postictal delirium has been classified by Kikuchi et. al. into four categories from no delirium, mild, moderate or severe delirium. Moderate to severe delirium needing restraints or sedative medication like benzodiazepines or Propofol was present 36% of patients, which is in line with older data. The more severe forms of delirium are easily recognised in clinical practice because of the need for intervention. When including mild forms, delirium was present in 52% of all patients in the study of Kikuchi et al. In newer studies using a more sensitive tool (CAM-ICU, Confusion Assessment Method - Intensive Care Unit) to assess the presence of delirium, the rates are up to 65% at 10 minutes after ECT stimulation respectively 10 minutes after arrival in the post-anaesthesia care unit. CAM-ICU is a brief but sensitive test, which has been extensively validated in the intensive care setting. Therefore, it seems that postictal delirium is frequently underdiagnosed in clinical practice. As we know from the intensive care literature, even hypoactive forms of delirium are associated with higher complication rates and higher mortality and therefore cannot be neglected.

In previous small studies, premedication with promethazine, midazolam and dexmedetomidine successfully reduced incidence of postictal delirium. Dexmedetomidine, a highly selective, relatively short acting alpha2-agonist, has been more extensively studied in the setting of ECT and has recently been able to show his potency to reduce postictal delirium by a third when given as a bolus pre-induction in a randomised controlled trial.

In this prospective, randomised, placebo-controlled, triple-blind, single-centre, two-arm parallel groups superiority trial, the investigators aim to lower incidence and severity of postictal delirium and agitation using a pre-induction dose of 2 mcg/kg clonidine intravenously compared to placebo (sodium chloride). The investigators also hypothesise, that a pre-induction dose of clonidine will reduce incidence of postictal agitation, the need for sedative rescue medication and the need for short-acting antihypertensive medication. It therefore might increase patient safety and cost effectiveness without prolonging post-anaesthesia care unit stay or negatively affecting treatment efficacy.

Being tested
Clonidine, Placebo
Keywords
Electroconvulsive Therapy, ECT, Clonidine, Postictal Delirium, Postseizure Delirium, Postictal Agitation, Postseizure Agitation, CAM-ICU, RASS
Medical subject headings
Depressive Disorder, Major, Catatonia, Bipolar Disorder

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • ClonidineDrug

    Also called Verum

    Clonidine 2mcg/kg Body Weight diluted in 100ml sodium chloride 0.9% compared to placebo (sodium chloride 0.9% alone) given over 10 minutes, 10 minutes prior to electroconvulsive therapy.

  • PlaceboDrug

    Sodium chloride 0.9% 100ml given over 10minutes, 10 minutes prior to electroconvulsive therapy.

Study groups in NCT04828226
Study groupRoleWhat they receive
InterventionExperimentalThe study drug (clonidine 2 mcg/kg) is diluted in 100 ml sodium chloride 0.9 % by trained post-anaesthesia care staff not involved in the study. At admission, electrocardiogram, non-invasive blood pressure and pulse oximetry is installed, a peripheral venous line established and supplemental oxygen applied. The study drug will be given intravenously over 10 minutes at least 10 minutes before induction of anaesthesia. Electroconvulsive therapy will be conducted according to hospital standard (Etomidate 0.2 mg/kg, Suxamethonium 1.0 mg/kg, isolated limb technique, THYMATRON® SYSTEM IV, Somatics Inc., Lake Bluf, Illinois, USA) adjusted to the patient's condition. Seizure quality will be assessed, prolonged seizure activity terminated with propofol 0.2 - 0.3 mg/kg. Severe agitation (Richmond Agitation and Sedation Score (RASS) > 1) needing intervention will be treated with propofol or lorazepam. Patients will be assessed for delirium using CAM-ICU at 20 minutes after induction.
Receives: Drug: Clonidine
ControlPlacebo comparatorThe placebo will be created by diluting 1ml of sodium chloride 0.9% in 100ml of sodium chloride in a sterile manner prior to application. The container will be identically labelled as the verum. The placebo will be applied by the same team members named above via the same route (intravenously), with the same speed and the same timing. All other parts of the procedure are identical as to the procedure described above.
Receives: Drug: Placebo

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Incidence of delirium after electroconvulsive therapy over all (twelve) ECT sessions

    The primary outcome is delirium after electroconvulsive therapy over all (twelve) ECT sessions. The presence of delirium will be assessed using Confusion Assessment Method - Intensive Care Unit (CAM-ICU). To be able to perform the test correctly, the patient must be awake enough. This will be assessed using the Richmond-Agitation-Sedation-Scale (RASS) first ranging from -5 (unarousable) to +4 (combative)

    Measured: 20 minutes after muscle relaxation

Secondary outcomes (17)
  1. Incidence of mild agitation

    RASS +1, needing verbal command or short restraint < 1 minute

    Measured: post-anaesthesia care unit stay (up to 2 hours)

  2. Incidence of severe agitation

    RASS > 1, needing restraint > 1 minute or rescue medication)

    Measured: post-anaesthesia care unit stay (up to 2 hours)

  3. Use of rescue medication

    medication, dose, route

    Measured: post-anaesthesia care unit stay (up to 2 hours)

  4. Duration of seizure activity

    seconds

    Measured: during procedure (estimated to be on average 10-15 minutes)

  5. Quality of seizure activity

    ideal, sufficient, insufficient

    Measured: during procedure (estimated to be on average 10-15 minutes)

  6. Seizure Quality Index

    Seizure Quality Index (Kranaster et al., Eur Arch Psychiatry Clin Neurosci 2018) ranging from 0 to 5. Higher index indicates better response to treatment.

    Measured: during procedure (estimated to be on average 10-15 minutes)

  7. Need for seizure terminating medication

    medication, dose, route

    Measured: during procedure (estimated to be on average 10-15 minutes)

  8. Total number of electroconvulsive therapy sessions

    number

    Measured: whole treatment course (12 ECT sessions, about 4 weeks)

  9. Reason for terminating or continuing the electroconvulsive series

    failure, response, remission, other reason

    Measured: whole treatment course (12 ECT sessions, about 4 weeks)

  10. Length of post-anaesthesia care unit stay

    minutes

    Measured: post-anaesthesia care unit stay (up to 2 hours)

  11. Incidence of desaturation

    Oxygen saturation by pulse oximetry < 75%, irrespective of duration

    Measured: post-anaesthesia care unit stay (up to 2 hours)

  12. Incidence of hypotension

    any measurement with mean arterial pressure < 55 mmHg

    Measured: during procedure (estimated to be on average 10-15 minutes)

  13. Incidence of bradycardia

    heart rate < 50 bpm for more than 1 minute

    Measured: post-anaesthesia care unit stay (up to 2 hours)

  14. Cardiovascular changes needing intervention

    number and type

    Measured: post-anaesthesia care unit stay (up to 2 hours)

  15. Use of cardiovascular medication

    medication, dose, route

    Measured: post-anaesthesia care unit stay (up to 2 hours)

  16. Adverse events potentially attributable to ECT

    diagnosis

    Measured: whole treatment course (12 ECT sessions, about 4 weeks)

  17. Adverse events potentially attributable to Study Drug

    diagnosis

    Measured: whole treatment course (12 ECT sessions, about 4 weeks)

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted1 Apr 2021
  2. Study start27 Apr 2021
  3. Primary completion16 May 2026
  4. Study completion16 May 2026

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 4
Primary purpose
Prevention
Allocation
Randomised
Intervention model
Parallel groups
Model description
This is a prospective, randomised, placebo-controlled, triple blind, single-centre, two-arm parallel groups superiority trial assessing incidence and severity of postictal delirium.
Masking
Quadruple blind
Who is masked
Participant, Care provider, Investigator, Outcomes assessor
Enrolment
130 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04828226
Sponsor's protocol ID
BECD-3-21
Acronym
ECaTa
Status last verified
May 2026
First submitted
30 Mar 2021
Last updated
19 May 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A Phase 4 study testing Clonidine in people with Major Depressive Disorder and Catatonia, run by Insel Gruppe AG, University Hospital Bern at 1 site in Switzerland.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 11 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 19 May 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Switzerland. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 4 studies take place after a treatment is approved, to learn more about its long-term benefits and risks in everyday use.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Incidence of delirium after electroconvulsive therapy over all (twelve) ECT sessions (time frame: 20 minutes after muscle relaxation). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 19 May 2026.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in