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:
2025-12-26 @ 10:44 PM
Ignite Modification Date:
2025-12-26 @ 10:44 PM
NCT ID:
NCT02261012
Eligibility Criteria:
CRPS-patients
Inclusion Criteria:
* Unilateral pain on the upper limbs, based on a scintigraphic ensured CRPS (average pain in the last 4 weeks ≥ 3 in pain Detect)
* Pain history \< 1 year
Exclusion criteria:
* Bilateral pain on the upper limbs
* Inadequate knowledge of the german language in speaking and writing
* Acute psychiatric sickness
* Polyneuropathy
* Any added neuropathic sickness on the not affected upper limb sight
* Intolerable pain during the testing
* Injuries within the tested areal
* Acute injuries on the hand
* Pregnancy
* Missing informed consent
CTS-patients
Inclusion Criteria:
* Unilateral pain on the upper limbs, based on a scintigraphic ensured CRPS (average pain in the last 4 weeks ≥ 3 in pain Detect)
* Pain history \< 1 year
Exclusion criteria:
* Bilateral pain on the upper limbs
* Inadequate knowledge of the german language in speaking and writing
* Acute psychiatric sickness
* Polyneuropathy
* Any added neuropathic sickness on the not affected upper limb sight
* Intolerable pain during the testing
* Injuries within the tested areal
* Acute injuries on the hand
* Pregnancy
* Missing informed consent
Healthy subjects
Inclusion Criteria:
* Age \> 18 years
* Written consent
Exclusion criteria:
* Inadequate knowledge of the german language in speaking and writing
* Current pain
* Pain within in the last 14 days
* Any serious internistic medicin
* Any chronic skin disease
* Any central neural sickness
* Polyneuropathy
* Peripheral nerve lesion within the testing areal
* Any radiculopathy with permanent pain (in the last 3 months)
* Any psychiatric sickness
* Migraine ( at least one attack in the last 24 h)
* Repeating headache (in the last 3 month on \>5 days/month)
* Taking any analgesics in the last 14 days
* Taking triptans in the last 24 months
* Taking any psychotropic's in the last 3 months
* Any repeated taking of medication, including amber or different psychostimulants (excluding contraceptives)
* Taking of any prescription and non-prescription drugs (except contraceptives) in the last 7 days or 5 half-life periods(which is always longer) before including into the study
* Achilles reflex absent or within in the side-difference pathologic hypoactive or hyperactive
* pallaesthesia \<5/8 (\<4/8 at \>60 years) on the internal malleolus on both sides
* abuse of alcohol or medications/drugs (corresponding to the DSM IV criteria)
* joining a medical study \<30 days before inclusion into the current study
* jet lag, irregular work schedule, sleep deprivation within the last 3 days
* change of intestity during physical activity, e.g. beginning an activity in the last weeks before inclusion into the current study
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT02261012
Study Brief:
Protocol Section:
NCT02261012