A multi-centre, double-blind, placebo-controlled, randomised, parallel groupclinical trial to evaluate efficacy and safety of Actovegin® in diabetic type 2patients with symptomatic diabetic peripheral polyneuropathy - Actovegin® versus placebo in patients with diabetic polyneuropathy

• Conditions: Diabetic Polyneuropathy; MedDRA version: 8.1Level: LLTClassification code 10012685Term: Diabetic polyneuropathy

• Registration Number: EUCTR2006-004007-19-AT
• Lead Sponsor: ycomed Austria GmbH

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2006-10-19
• Last Update Posted: 19 March 2012

Recruitment & Eligibility

• Status: ot Recruiting
• Sex: All
• Target Recruitment: 550

Inclusion Criteria

1. Has the patient given informed consent according to local requirements before any trial related activities? A trial related activity is any procedure that would not have been performed during the routine management of the patient.
2. Is the patient aged = 18 to = 65 years?
3. Does the patient suffer from type 2 diabetes mellitus?
4. Has the patient evidence of symptomatic diabetic peripheral polyneuropathy, i.e. TSS =6 and NIS-LL = 2?
5. Is the patient’s VPT measured to = 30V?
6. Has the patient adequate circulation to the foot as evidenced by a palpable pulse on posterior tibialis artery and dorsal artery of foot?
7. Is the HbA1C level less than 10%?
8. Is the patient able to make frequent clinic visits over the trial period?

For patients receiving tricyclic antidepressants, anticonvulsants, mexiletine or neuroleptics as treatment of neuropathic pain:
9. Has the regimen been stable within the last month?

For female patients of childbearing potential (childbearing potential is considered until menopause has lasted more than 12 months):
10. Does the patient use an acceptable contraceptive method (hormonal pills, patches, implants, injections or intrauterine device)?
11. Is the pregnancy test negative before the 1st dose of IMP?
(Surgically hysterectomised and surgically successfully sterilized females may be included on the same conditions as male patients).
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range
F.1.3 Elderly (>=65 years) no
F.1.3.1 Number of subjects for this age range

Exclusion Criteria

1. Does the patient suffer from known allergy towards Actovegin or similar preparations?
2. Has the patient asymmetrical neuropathy of the trunk or proximal lower limbs?
3. Does the patient suffer from diabetic foot ulceration or infections?
4. Does the patient suffer from diabetic amyotrophy?
5. Does the patient suffer from decompensated cardiac insufficiency, pulmonary oedema, oliguria, anuria, generalised oedema?
6. Does the patient suffer from polyneuropathy due to other underlying causes?
7. Has the patient been hospitalised due to diabetic polyneuropathy within the last month?
8. Has the patient participated in any other trial with an Investigational Medicinal Product (IMP) or device within 30 days before inclusion in this trial?
9. Has the patient ever used medications that may be etiological factors for neuropathy, such as isoniazid, nitrofurantoin, vincristine and phenytoin?
10. Has the patient used cerebrolysin or a-lipoic acid or received Transcutaneous Electric Nerve Stimulation (TENS) or acupuncture within the last month?
11. Has the patient received opiates as treatment of his / her diabetic polyneuropathy within the last month?
12. Does the patient suffer from any malignancy?
13. Is the patient nursing?
14. Does the patient suffer from any mental, psychiatric or other conditions that may
compromise data collection and understanding of written and verbal information given in the trial?
15. Does the patient suffer from present and / or previous chronic alcohol abuse?
16. Is there any anamnestic evidence of hypothyroidism?
17. Is there any anamnestic evidence of vitamin B12 deficiency?
18. Does the patient suffer from an impaired renal function with high blood urea nitrogen (BUN) and / or increased serum creatinine (>120 µmol/L)?

Study & Design

• Study Type: Interventional clinical trial of medicinal product
• Study Design: Not specified