Eligibility Module

Eligibility Module

The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.

Eligibility Module path is as follows:

Study -> Protocol Section -> Eligibility Module

Eligibility Module


Ignite Creation Date: 2025-12-24 @ 11:37 PM
Ignite Modification Date: 2025-12-24 @ 11:37 PM
NCT ID: NCT00370656
Eligibility Criteria: Inclusion Criteria: 1. 18 years of age or above 2. Have a diagnosis of Diabetes mellitus for at least a year 3. Agree not to smoke whilst resident in the CRC 4. Able to understand the patient information sheet and provide written informed consent 5. Score above 12 on the LANSS 6. Have neuropathic pain of diabetic origin 7. Score above 25 on MMSE 8. Willing to withdraw, under the guidance of their diabetologist, from any current pain medication prior to their first visit to the sleep laboratory. Duration of withdrawal will be at least equivalent to 5 half-lives and will be of a relevant duration given the particular medication used. Exclusion Criteria: 1. There is evidence of an end stage disease of a major system (hepatic, renal, respiratory, haematologic (PA), immunologic, cardiovascular, inflammatory, rheumatology, active infections, peripheral vascular disease, untreated endocrine(hypothyroid) 2. There is evidence of a recent ischaemic event 3. There is evidence of recurrent and/or severe hypoglycemia requiring assistance in last 3 years 4. Evidence of sleep pathology that would interfere with the assessment of treatment (assessed on habituation night) 5. Currently receiving treatment for malignancy 6. Suffer from seizures including epilepsy 7. There is evidence of a history of dependence on or abuse of alcohol/recreational drugs 8. Need to use a wheel chair (incompatible with studies in a sleep laboratory) 9. Involved in a clinical trial in last 3 months 10. Pregnant, lactating or inadequate contraception 11. Vision inadequate for the performance tests (as assessed at screening) 12. Colour Blind 13. Will not co-operate with study procedures 14. Will not give permission to inform GP
Healthy Volunteers: False
Sex: ALL
Minimum Age: 18 Years
Study: NCT00370656
Study Brief:
Protocol Section: NCT00370656