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Sensory Mapping Following Video-assisted Thoracic Surgery

Rigshospitalet logo

Rigshospitalet

Status

Unknown

Conditions

Paresthesia
Pain
Dysesthesia

Study type

Observational

Funder types

Other

Identifiers

NCT01375283
H4-2010-118#2

Details and patient eligibility

About

This is a prospective observational cohort study on changes in sensory mapping.

Enrollment

48 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age < 18 years old
  • Elective lung cancer surgery (VATS)

Exclusion criteria

  • does not understand Danish
  • cognitive reduction
  • bilateral procedure planned
  • previous thoracic surgery
  • pregnant or nursing
  • known nerve affection from other cause
  • alcohol/substance abuse
  • inability to cooperate to pain scoring/sensory examination
  • > 5 mg methylprednisolone/day

Trial design

48 participants in 1 patient group

lung cancer surgery

Trial contacts and locations

1

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Central trial contact

Kim Wildgaard, MD

Data sourced from clinicaltrials.gov

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