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Open Label Study of Duloxetine for the Treatment of Phantom Limb Pain

Pilot Study of Use of Duloxetine for the Treatment of Phantom Limb Pain

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00425230
Enrollment
15
Registered
2007-01-22
Start date
2007-01-31
Completion date
2007-06-30
Last updated
2022-08-12

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

Conditions

Chronic Phantom Limb Pain

Brief summary

This is a study to assess the possible benefit of duloxetine in the treatment of chronic phantom limb pain.

Interventions

DRUGDuloxetine

Sponsors

Baylor College of Medicine
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

1. Chronic PLP \> 6 months 2. Short-Form McGill Pain Questionnaire Sensory Pain Rating Index raw score ≥ 16 3. Age ≥ 18 years old 4. Inpatient or Outpatient 5. Able to come to all appointments, in the opinion of the investigator 6. Able to give informed consent, in opinion of investigator

Exclusion criteria

1. Current Major Depressive disorder, Anxiety Disorder, or Psychotic disorder assessed by the Mini International Neuropsychiatric Interview (MINI) 2. Substance abuse or dependence within the last six months, as assessed by the MINI 3. Known Diabetes Mellitus to exclude diabetic peripheral neuropathy 4. History of coronary artery disease, hepatic disease, renal disease 5. Other pain syndromes 6. Any unstable medical conditions in the opinion of the investigator 7. Other psychotropic medications excluding hypnotics

Design outcomes

Primary

MeasureTime frame
McGill Short Form Pain Questionairre

Secondary

MeasureTime frame
Fiser Side effect scale
visual analog pain scale
Present Pain intensity
Tylenol # 3 consumption

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026