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Evaluation of the analgesic effects of duloxetine in burn patients

Evaluation of the analgesic effects of duloxetine in burn patients

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017051422637N4
Enrollment
42
Registered
2017-05-31
Start date
2017-01-30
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

Burn. Burns and corrosions of external body surface, specified by site

Interventions

Intervention 1: Intervention: a 60 mg oral capsule of duloxetine per day. Intervention 2: Control: No treatment.
Treatment - Drugs
Intervention: a 60 mg oral capsule of duloxetine per day

Sponsors

Vice chancellor for research, Kerman University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to 75 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Burn patients requiring hospitalization for at least one week Exclusion criteria: Bipolar mood disorder; consuming monoamine oxidase inhibitor drugs, three cyclic antidepressant drugs, tramadol, buspirone, triptan drugs, lithium, ondansetron, potent inhibitors of cytochrome P450 (CYP450) 2D6 and CYP450 1A2; creatinine clearance less than 30 ml per minute; hepatic failure; uncontrolled epilepsy; thrombocytopenia

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Severity of pain. Timepoint: At baseline and every other day. Method of measurement: Visual Analog Scale.;Severity and quality of pain. Timepoint: At baseline and every other day. Method of measurement: Neuropathic Pain Scale.

Secondary

MeasureTime frame
Dose of other analgesic drugs. Timepoint: At the end of the study. Method of measurement: Recording the dose of other analgesics.;Adverse effects. Timepoint: During the study. Method of measurement: Patient report.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAli Najafi

Kerman University of Medical Sciences

najafiali57@yahoo.com+98 34 3132 5000

Outcome results

None listed

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