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Effects of transcutaneous pulsed radiofrequency on patients with advanced cancer

Effects of transcutaneous pulsed radiofrequency on patients with advanced cancer - Transcutaneous pulsed radiofrequency applied to cancer patients

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON46593
Enrollment
15
Registered
2018-08-16
Start date
2019-01-10
Completion date
Unknown
Last updated
2024-06-11

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

Conditions

advanced stage cancer metastasis

Interventions

Transcutaneous pulsed radiofrequency (tPRF) treatment is non-invisave and painless. It has been used as a pain-relief procedure with no known complications or side effects. tPRF will be applied eve

Sponsors

Radboud Universitair Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: 1) >= 18 years of age; 2) patients with advanced-stage colorectal, breast, prostate or ovarian cancer; 3) presently no longer responding to systemic treatment, and no other standard oncological treatment can be applied anymore (i.e. a patient is strictly in a clear palliative trajectory). 4) history of tumor marker corresponding with disease progression on imaging; 5) history of tumor marker responding to previous oncological treatment; 6) patients able and willing to give written informed consent and comply with the requirement of the study protocol; 7) life expectancy at least 3 months.

Exclusion criteria

Exclusion criteria: 1) treatment with any cancer therapy, including but not limited to chemotherapy and radiation therapy, within 4 weeks before baseline; 2) in the use of critical measuring devices, large metal implants or active implants like a pacemaker; 3) pregnant.

Design outcomes

Primary

MeasureTime frame
Tumor markers - Carcinoembryonic antigen (CEA) for colorectal cancer; - Carcinoma antigen 15.3 (CA15.3) for breast cancer; - Prostate-specific antigen(PSA) for prostate cancer: - Carcinoma antigen 125 (CA125) for ovarian Cancer.

Secondary

MeasureTime frame
Pain intensity will be assessed using numeric rating scale (NRS); Quality of Life (QOL) will be assessed by -EORTC quality of life questionnaires QLQ-C30 and cancer-specific module; -Edmonton Symptom Assessment System (ESAS).

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)