Skip to content

A comparison of combined Endoscopic ultrasound-guided radiofrequency ablation using Endoscopic ultrasound-guided radiofrequency ablation electrode and chemotherapy versus chemotherapy alone in locally advanced pancreatic cancer: a phase II/III randomized controlled trial

A comparison of combined EUS-guided radiofrequency ablation using EUSRA RF electrode and chemotherapy vs. chemotherapy alone in locally advanced pancreatic cancer: a phase II/III randomized controlled trial

Status
Recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20250117003
Enrollment
26
Registered
2025-01-17
Start date
2025-01-16
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Scheduling follow-up appointments and treatment for patients can be challenging

Interventions

i. Radiofrequency Ablation (RFA) via Endoscopic Ultrasound: 1. The equipment used includes an ultrasound endoscope (EG-3870K: Pentax Corporation and Ultrasound Scanner NOBLUS: Hitachi), a Monopolar RF
Experimental Procedure/Surgery,Active Comparator Procedure/Surgery
Radiofrequency Ablation (RFA) group,Chemotherapy group

Sponsors

Ratchadapisek Somphote Endowment Fund Chulalongkorn University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1.Patients diagnosed with advanced pancreatic adenocarcinoma confirmed by pathology, 2. Inoperable as determined by radiologic findings or expert surgeon opinion (AJCC 8th stage III, TNM stage T1-3 or N2, T4 any N, M0). 3. ECOG performance status 2.

Exclusion criteria

Exclusion criteria: 1. Patients for whom RFA cannot be performed due to technical issues. 2. Pregnant patients. 3. Patients previously treated for pancreatic cancer with standard therapies. 4. Patients with uncorrectable coagulopathy. 5. Patients who do not consent to participate.

Design outcomes

Primary

MeasureTime frame
survival rate 6-month lab results (Liver Function Tests), side effects (Nausea and Vomiting), pain medication dosage, and quality of life

Secondary

MeasureTime frame
adverse effects (Hematologic, Gastrointestinal) 6 months European Organisation For Research And Treatment Of Cancer-Quality Of Life (Functioning Scales, Symptom Scales)

Countries

Thailand

Contacts

Public ContactPradermchai Kongkam

chulalongkorn university

kongkam@hotmail.com022564356

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026