Skip to content

Differences in Pain Processing Between Men and Women

Differences in Sensitization Between Men and Women After Cutaneous Thermal Stimuli

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05031286
Enrollment
66
Registered
2021-09-01
Start date
2021-05-01
Completion date
2022-12-31
Last updated
2023-04-11

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

Conditions

Central Sensitisation

Keywords

central sensitisation, central sensitization, nociception, withdrawal reflex, heat pain, secondary hyperalgesia

Brief summary

Many chronic pain conditions show clear differences between between men and women, such as reported pain intensities or treatment effects, with chronic pain conditions being generally more frequent in women. Yet, the underlying mechanisms causing these differences are poorly understood. Central sensitization (CS) is considered one important mechanism in pain patients which differs between female and male patients. The central hypothesis is that already in the healthy population CS processes are more pronounced in women than in men.

Interventions

OTHERCutaneous thermal stimuli

Application of thermal stimuli of different intensities to the skin

Sponsors

Balgrist University Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

* good general health * able to give informed consent

Exclusion criteria

* pain complaints for more than two consecutive days over the past three months * any major medical or psychiatric condition (e.g. heart disease, major depressive disorder) * any chronic pain condition * inability to follow study instructions * consumption of stimulants, drugs, or analgesics within the past 24 hours * scar tissue or generally reduced sensitivity in the designated testing site areas

Design outcomes

Primary

MeasureTime frameDescription
Change in spatial extent of mechanical hypersensitivity after intervention w.r.t. baseline10-20 minutes before intervention (baseline) and 20-30 minutes after interventionMapping of hypersensitivity in cm2 of sensitized skin area using two quantitative sensory testing tools (256mN von Frey filament and 200-400mN brush) before and after intervention
Changes to the nociceptive withdrawal reflex (NWR) after intervention w.r.t. baseline5-10 minutes before intervention (baseline) and 30-35 minutes after interventionRepetitive suprathreshold elicitation of the NWR to monitor its characteristics (such as magnitude and number of responses) before and after intervention

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026