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Relevance of DNIC (diffuse noxious inhibitory Control) for pain and hyperalgesia following an incision in healthy volunteers.

Relevance of DNIC (diffuse noxious inhibitory Control) for pain and hyperalgesia following an incision in healthy volunteers. - Incision CPM Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00014291
Enrollment
24
Registered
2018-03-16
Start date
2010-05-10
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

ENDOGENESCHMERZHEMMUNGUNDSENSITISIERUNGDIEZUAKUTEUNDCHRONSICHESCHMERZENFHRENKNNEN

Interventions

Group 1: In healthy male volunteers the CPM Paradigma (conditioned pain Modulation, formerly called DNIC - diffuse noxious inhibitory control) is evaluated on day one, using a contact heat stimulus ap

Sponsors

Universitätsklinikum Münster, Klinik für Anästhesiologie, operative Intensivmedizin und Schmerztherapie
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: healthy, male volunteers

Exclusion criteria

Exclusion criteria: Patients under 18 years of age, intake of analgesics or psychopharmaca, chronic pain condition, neurological condition, diabetes mellitus, hypertension

Design outcomes

Primary

MeasureTime frame
Difference in spontaneous pain after incision (evaluated with numeric rating scale 0-100 directly after incision) by comparing incisional pain with parallel activation of conditioned pain modulation (contralateral Hand in a noxious cold water bath during incision) and incisional pain without parallel activation of conditioned pain modulation (contralateral hand in a non-noxious lukewarm water bath during incision).

Secondary

MeasureTime frame
Correlation between Conditioned Pain Modulation and thermal and mechanical thresholds and mechanical pain sensitivity before and 1, 3, 9 and 27 hours after induction of the experimental incision; Differences between incison during CPM and without CPM regarding the above mentioned parameters before and 1, 3, 9 and 27 hours after induction of the experimental incision

Countries

Germany

Contacts

Public ContactEsther Pogatzki-Zahn

Universitätsklinik Münster, Klinik für Anästhesiologie, operative Intensivmedizin und Schmerztherapie

pogatzki@anit.uni-muenster.de0251 8347261

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026