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Phase 4 N=33 Randomized Single-blind Treatment

Efficacy of Intercostal CryoAnalgesia in Robotic Lung Resection

Pain, Postoperative · Lung Diseases

Enrolled (actual)
33
Serious AEs
0.0%
Results posted
Jan 2026
Primary outcome: Primary: Change in Visual Analogue Scale (VAS) Pain Score — 4.94; 7.50; 4.57; 6.25 scores on a scale

Study Design & Population

Study type
Interventional
Phase
Phase 4
Interventions
Intercostal Nerve Cryoablation (Device); Patient-controlled analgesia (PCA) (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Medical College of Wisconsin
Primary completion
Oct 2024

Outcome Measures

OutcomeResultp-value
PRIMARY
Change in Visual Analogue Scale (VAS) Pain Score
4.94; 7.50; 4.57; 6.25; 4.14; 5.44
PRIMARY
Pain Medication Use
6.47; 24.38; 8.24; 23.44; 3.00; 19.69
SECONDARY
M.D. Anderson Symptom Inventory (MDASI) Score
13.82; 10.88; 40.47; 34.50; 37.53; 25.19
SECONDARY
Leeds Assessment of Neuropathic Symptoms and Signs (LANSS) Score
0; .13; 8.06; 6.20; 8.33; 3.33

Summary

This is a single center, single surgeon, prospective, randomized trial examining the addition of Cryo Nerve Block during robot assisted thoracoscopic anatomic lung resection surgery

Eligibility Criteria

Inclusion Criteria

  • 18-85 years of age
  • Acceptable surgical candidate
  • Willing and able to return for scheduled follow-up visits

Exclusion Criteria

  • Patients undergoing or requiring conversion to thoracotomy
  • Patients with chronic pain syndromes requiring treatment within the last year
  • Patients with a history of illicit drug use
  • Patients with a history of heavy alcohol use in the last five years as determined by the principal investigator
  • Patients currently using opioids
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT05144828). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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