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NOT YET RECRUITING
NCT07671612
NA

PBM Patch for Postoperative Pain Relief After Urological Surgery

Sponsor: National Taiwan University Hospital

View on ClinicalTrials.gov

Summary

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).

Official title: A Double-blind Randomized Controlled Clinical Study of the PBM Patch for Postoperative Pain Relief After Urological Surgery

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

300

Start Date

2026-07-01

Completion Date

2028-03-31

Last Updated

2026-06-26

Healthy Volunteers

No

Interventions

DEVICE

Super Vi PBM Patch - Soothing

A photobiomodulation (PBM) patch designed for postoperative pain relief. The patch will be applied immediately upon arrival in the post-anesthesia care unit (PACU) after urological surgery.

DEVICE

Super Vi PBM Patch - Soothing EX

A photobiomodulation (PBM) patch designed for postoperative pain relief. The patch will be applied immediately upon arrival in the post-anesthesia care unit (PACU) after urological surgery.

DEVICE

Placebo Patch

An placebo patch visually identical to the study patches but without therapeutic photobiomodulation delivery. The patch will be applied immediately upon arrival in the post-anesthesia care unit (PACU) after urological surgery.

Locations (2)

National Taiwan University Hospital

Taipei, Taipei City, Taiwan

National Taiwan University Cancer Center

Taipei, Taipei City, Taiwan