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Effects of Low Dose Fentanyl Supplementation of Reduced Dose Propofol during Electroconvulsive Therapy

Effects of Low Dose Fentanyl Supplementation of Reduced Dose Propofol during Electroconvulsive Therapy

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20201127005
Enrollment
Unknown
Registered
2020-11-27
Start date
2015-09-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

psychiatric patients who receiving electroconvulsive therapy Electroconvulsive therapy Fentanyl Hemodynamic response Propofol Thiopental Seizure duration

Interventions

receiving thiopental 2 mg/kg,receiving propofol 1 mg/kg,fentanyl 0.3 mcg/kg&#44
followed by propofol 0.5 mg/kg.
Thiopental group,Propofol group,Fentanyl plus propofol group

Sponsors

Faculty of Medicine, Ramathibodi Hospital
Lead Sponsor
Faculty of Medicine&#44
Collaborator
Ramathibodi Hospital
Collaborator

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: adults, aged 18-65 years old and scheduled for bilateral ECT treatment.

Exclusion criteria

Exclusion criteria: patients who had a history of cardiovascular or cerebrovascular disease, poorly controlled hypertension, pregnancy, obesity (body mass index > 30 kg/m2), and had a contraindication to use thiopental, propofol, fentanyl, or succinylcholine.

Design outcomes

Primary

MeasureTime frame
seizure duration Pre-dose, 1 min,2 min,3 min,4 min,5 min,6 min,7 min,8 min,9 min,10 min Post-dose EEG,blood pressure in,3 min,4 min,5 min,6 min,7 min,8 min,9 min,10 min Post-dose mmHg,blood pressure Pre-dose, 1,2,3,4,5,6,7,8,9,10 Post-dose mmHg,Oxygen satuaration in,3 min,4 min,5 min,6 min,7 min,8 min,9 min,10 min Post-dose pulse oxymeter ,heart rate in,3 min,4 min,5 min,6 min,7 min,8 min,9 min,10 min Post-dose EKG

Secondary

MeasureTime frame
BIS index in,3 min,4 min,5 min,6 min,7 min,8 min,9 min,10 min Post-dose BIS

Countries

Thailand

Contacts

Public ContactVarinee Lekprasert

Faculty of Medicine, Ramathibodi Hospital, Mahidol University

varinee.lek@mahidol.ac.th+66817212292

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026