PBM Patch for Postoperative Pain Relief After Urological Surgery

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorNational Taiwan University Hospital

About this trial

This study is a prospective, randomized, double-blind, placebo-controlled clinical study designed to evaluate the efficacy and safety of a photobiomodulation (PBM) patch (Super Vi PBM Patch - Soothing) and an enhanced PBM patch (Super Vi PBM Patch - Soothing EX), compared with a placebo patch, for postoperative pain relief following urological surgery, including nephroureterectomy with bladder cuff resection (NU+BCR) and adrenalectomy (ADRX).

Eligibility criteria

Qualifiers

Patients aged 18 years or older undergoing unilateral nephroureterectomy with bladder cuff excision, or adrenalectomy (tumor size < 3.5 cm).

Patients who are capable of clear verbal communication.

Patients who are able to provide written informed consent.

Disqualifiers

Individuals with photosensitive constitution or those currently using photosensitizing medications.

Individuals with a known history of severe allergy or contact dermatitis to medical adhesive patches or tapes.

Patients with severe psychiatric illness or cognitive impairment.

Long-term or high-dose opioid users.

Trial design

Treatments tested in this trial

  • Super Vi PBM Patch - Soothing
  • Super Vi PBM Patch - Soothing EX
  • Placebo Patch

Treatment groups

300 Participants
are divided into 3 treatment groups