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Evauating the effects of oral N-acetylcysteinas in comparing with pregabalin for pain managementinpatients with painful diabetic neuropathy.

Evauating the effects of oral N-acetylcysteinas in comparing with pregabalin for pain managementinpatients with painful diabetic neuropathy.

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180814040795N1
Enrollment
140
Registered
2018-11-11
Start date
2018-08-21
Completion date
Unknown
Last updated
2019-01-14

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

Conditions

Diabetic Polyneuropathy. Type 2 diabetes mellitus with diabetic polyneuropathy

Interventions

Intervention 1: Intervention group: 600mg of effervescent tablet of N-acetyi cysteine every12 hours for 8 weeks . Intervention 2: Control group: 75mg of pregabalin every 12 hours for 8 weeks .

Sponsors

Hamedan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 70 Years

Inclusion criteria

Inclusion criteria: Age 30 to 70 years old History of DM2 at least one year ago Hb A1C less than or equal to 9 Diabetic Neuropathy with NDS score greater than or equal to 6; VAS Score fore pain at least 4 and NSS score greater than or equal to 5. Glomerular filteration rate more than 30cc/min

Exclusion criteria

Exclusion criteria: Type 1 diabetes Pregnancy or breast feeding Diabetic foot ulcer Neuropathy for reason other than diabetes History of cerebrovascular disease and discopathy Use other medications to relieve symptoms of neuropathy Use of alcoholic drink or opioids

Design outcomes

Primary

MeasureTime frame
Visual analogue scale. Timepoint: Before intervention, the end of the first month and the end of the second month. Method of measurement: Indicator.;Sleep interference score. Timepoint: Before intervention, the end of the first month and the end of the second month. Method of measurement: Questionnaire.;Patient global impression of change. Timepoint: Before intervention and 2 months after intervention. Method of measurement: Questionnaire.;Clinical global impression of change. Timepoint: Before intervention and 2 months after intervention. Method of measurement: Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFirozeh Sajedi

Hamedan University of Medical Sciences

firozeh.sajedi@yahoo.com+98 81 3838 0704

Outcome results

None listed

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