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A comparison of concurrent chemo-radiotherapy plus hyperthermia versus concurrent chemo-radiotherapy in locally advanced cervical cancer patients: A randomized controlled trial

A comparison of concurrent chemo-radiotherapy plus hyperthermia versus concurrent chemo-radiotherapy in locally advanced cervical cancer patients: A randomized controlled trial

Status
Unknown
Phases
Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20180711002
Enrollment
90
Registered
2018-07-11
Start date
2018-06-01
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

&#45

Interventions

Patients receive radiation five days per week&#44
total radiation fraction 25&#45
30 fraction. Patients receive weekly chemotherapy such as cisplatin or carboplatin during radiation therapy,Patients receive radiation five days per week&#44
30 fraction. Patients receive weekly chemotherapy such as cisplatin or carboplatin during radiation therapy Patients receive weekly hyperthermia during radiation therapy
concurrent chemoradiotherapy,concurrent chemoradiotherapy plus hyperthermia

Sponsors

Chulabhorn Hospital, HRH Princess Chulabhorn College of Medical Science, Chulabhorn Royal Academy
Lead Sponsor
Thermtech Medical Co.&#44
Collaborator
Ltd.
Collaborator

Eligibility

Sex/Gender
Female
Age
19 Years to No maximum

Inclusion criteria

Inclusion criteria: - CA cervix FIGO stage IB2, IIA2-IVA - Patho : squamous cell carcinoma, adenosquamous carcinoma or adenocarcinoma - Age more than 18 years - KPS > 70 - Treatment plan is concurrent chemoradiotherapy - No paraaortic lymph node metastasis - Adequate bone marrow and kidney function - No HIV history

Exclusion criteria

Exclusion criteria: - Patients have cardiac pacemaker or metal prosthesis in their body - Patients received abdominal radiotherapy or chemotherapy - Distant metastases - Previous malignancy, except adequately treated non-melanoma skin cancer

Design outcomes

Primary

MeasureTime frame
Treatment response rate at least 3 months after completion of treatment percentage and exact probability test

Secondary

MeasureTime frame
local relapse-free survival, disease-free survival, overall survival 2 year Kaplan Meier Statistical Analysis, Log-rank test

Countries

Thailand

Contacts

Public ContactSunanta Rojwatkarnjana

Chulabhorn Hospital, HRH Princess Chulabhorn College of Medical Science, Chulabhorn Royal Academy

pukmd@hotmail.com0816264470

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026