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Comparative efficacy of Duloxetine versus Gabapantin in patients with painful diabetic peripheral neuropathy

Comparison the efficacy of Duloxetine versus Gabapantin in patients with painful diabetic peripheral neuropathy

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20161023030455N2
Enrollment
104
Registered
2018-08-06
Start date
2018-05-22
Completion date
Unknown
Last updated
2018-09-11

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

Conditions

painful diabetic peripheral neuropathy. Diabetic polyneuropathy

Interventions

Intervention 1: The gabapentin group receives the gabapentin at a dose of 300 mg per day. Then, the dose of 300 mg increases every three days to reach 900 mg per day (300 mg three times per day) and t

Sponsors

Vice chancellor for research of Ahvaz Jundishapur University of Medical Sciences Department of Neuro
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: aged>18 rule out other DDx. for peripheral neuropathy do nt use drug for treatment of DPNP duration of diabetes ranging from 1 to 15 years HbA1C less than 10 mg A pain score of at least 40 mm on the 100 mm visual analogue scale (VAS)

Exclusion criteria

Exclusion criteria: patients who were already on other medication for the treatment of DPNP one week prior to the study enrolment hepatic failure; ;renal failure with GFR<30 ml/min concurernt of psycologic disoeder cardiac arhythmia patients with established neuropathy due to other causes;, history of epilepsy drug abuse uncontoroled acute close angle Glocoma recent MI patients who did not give written informed consent pregnant or lactating women

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: Before treatment and 1,4 and 8 weeks after treatment. Method of measurement: visual analogue scale.

Secondary

MeasureTime frame
Sleep quality. Timepoint: Before treatment and 1,4 and 8 weeks after treatment. Method of measurement: Sleep interference score.;Changes in clinical status. Timepoint: 1,4and 8 weeks after treatment. Method of measurement: Clinical Global Impression of Change.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHosein Kaveiani

Ahvaz University of Medical Sciences

drkaveiani@gmail.com+98 66 4250 3340

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 21, 2026