CerviCALOR - Hyperthermia in Cervical Cancer Biopsies

CerviCALOR - Hyperthermia Induced Synthetic Lethality in Tumour Biopsies from Women with Cervical Cancer

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON27066

Enrollment

200

Registered

2019-05-21

Start date

2019-05-21

Completion date

Unknown

Last updated

2024-02-28

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

Conditions

Cervical Cancer

Interventions

None

laboratory investigations

Eligibility

Inclusion criteria

Inclusion criteria: • Adult women with cervical cancer (>18 years) • who will have an investigation under general anesthesia (or: under spinal anesthesia), • and who have given written informed consent for extra biopsies for research.

Exclusion criteria

Exclusion criteria: • Women = 18 years, • Or who will not have an investigation under general anesthesia for whatever reason, • Unwilling or unable to give written informed consent, either because of mental limitations or because of a language barrier

Design outcomes

Primary

Measure	Time frame
Tumour Response	—

Secondary

Measure	Time frame
DNA-repair modification	—

Contacts

Public ContactLukas Stalpers

AmsterdamUMC, location AMC

l.stalpers@amsterdamumc.nl+31-20-5664231

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)