In patients with painful diabetic neuropathy, total FIS score fell from 8.7 to 5.1 after 6 weeks with Cerebrolysin, and from 7.9 to 6.6 in the placebo group.
In plain wordsIn patients with diabetic neuropathy, symptom scores fell after Cerebrolysin and also fell in the placebo group.
- Peptide
- Cerebrolysin
- Outcome
- DecreaseTotal FIS score
- Study
n = 20
- Outcome group
- Pain · Nervous system and cognition
- Studied dose
- 20 ml daily · infusion · 10 daysAs given in this study (human).
Measurements
- FIS score
- 8.7 score
- start
- FIS score
- 5.1 score
- 6 weeks
- Reported +/- term for total FIS score
- 1.9 score
- Cerebrolysin, start of therapy; uncertainty type not stated
- Reported +/- term for total FIS score
- 2.2 score
- Cerebrolysin, after 6 weeks; uncertainty type not stated
- p value for total FIS score decrease
- < 0.001 p value
- Cerebrolysin, start of therapy versus after 6 weeks
- Total FIS score
- 7.9 score
- Placebo, beginning of therapy
- Reported +/- term for total FIS score
- 1.2 score
- Placebo, beginning of therapy; uncertainty type not stated
- Total FIS score
- 6.6 score
- Placebo, 6 weeks later
2 more measurements in the study.
Source sentences
Cerebrolysin was associated with a significant decrease in total FIS score from 8.7 +/- 1.9 at the start of therapy to 5.1 +/- 2.2 after 6 weeks (p < 0.001),
In contrast in the placebo group the total FIS score decreased only from 7.9 +/- 1.2 at the beginning to 6.6 +/- 1.1 (p < 0.05) 6 weeks later
2 context sentences(design, population, supporting numbers)
In a placebo-controlled longitudinal study we investigated the effect of that drug for treatment of painful diabetic neuropathy in 20 type-II diabetic patients (9 women, 11 men, mean age 63 +/- 9 years, duration of diabetes 14 +/- 7 years).
Patients received daily a cerebrolysin-infusion (20 ml in 500 ml Ringer) over a period of 10 days.