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Low field TMS as pain treatment as measured with quantitative sensory testing.

Low field TMS as pain treatment as measured with quantitative sensory testing.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON21962
Enrollment
100
Registered
2007-10-16
Start date
2007-11-01
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

1. Pain

Interventions

Transcraniele magnetische stimulatie met zwakke velden.

Sponsors

UMCG Postbus 196 9700 AD Groningen the Netherlands
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. 18-80 years old; 2. subjectively healthy; 3. neuropathic pain (patients only).

Exclusion criteria

Exclusion criteria: 1. Neurological (e.g. epilepsy) history (volunteers only); 2. Neurological history apart from neuropathic pain (patients only); 3. Psychiatric history; 4. Recent use (within four weeks) of antidepressants, antiepileptic drugs or prescription psychopharmaca; 5. Excessive use of: coffee (>10 units per day), alcohol (>10 units per day); 6. Recent use (within four weeks) of cannabis or any other non-prescription psychopharmaca; 7. Presence in the body of MRI incompatible implants, electronic implants (e.g. cardiac pacemakers),or connectors of electronic equipment (e.g. electrodes).

Design outcomes

Primary

MeasureTime frame
Safety and tolerability in healthy volunteers and patients: any self-reported experiences are recorded. Small neuropsychological tests are performed such as long number recollection and reverse recital of the months of the year. Neuropathic pain model in healthy volunteers and neuropathic pain in patients: visual analogue scale of pain intensity. Nociceptive pain model in healthy volunteers and patients: warmth detection threshold (oC) and heat pain threshold (oC).

Secondary

MeasureTime frame
During the pain studies (as opposed to the safety and tolerability studies where this is the main endpoint) all subjects are debriefed about whether any sensations were perceived during the experiment.

Contacts

Public ContactR. Kortekaas

Postbus 196

r.kortekaas@med.umcg.nl

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)