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Observational study on anesthesia practices in cancer patients undergoing electrotherapy of cancer tumors

ADMIRE study: Anaesthesia Decision and Management in IRreversible Electroporation procedures - ADMIRE study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2025/08/092514
Enrollment
89
Registered
2025-08-06
Start date
Unknown
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

Health Condition 1: C22- Malignant neoplasm of liver and intrahepatic bile ducts Health Condition 2: C25- Malignant neoplasm of pancreas Health Condition 3: C73- Malignant neoplasm of thyroid gland Health Condition 4: C45-C49- Malignant neoplasms of mesothelial and soft tissue Health Condition 5: C00-D49- Neoplasms

Interventions

Intervention1: Nil: Nil Intervention2: Nil: Nil Intervention3: Nil: Nil Control Intervention1: Nil: Nil

Sponsors

NIL
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All patients who underwent and will undergo Irreversible Electroporation procedure from 1st January 2020

Exclusion criteria

Exclusion criteria: Patient who refuse to consent in the prospective group of the study

Design outcomes

Primary

MeasureTime frame
To describe adverse events during Irreversible Electroporation at our centre- Tata memorial hospital, MumbaiTimepoint: 24 hours from start of the procedure (From induction of anaesthesia till end of IRE procedure and immediate postoperative)

Secondary

MeasureTime frame
Interference of IRE on Electrocardiography monitoringTimepoint: 24hours from start of procedure (induction of anaesthesia);Effect of electrical pulses on Bispectral Index monitoringTimepoint: 24 hours from start of procedure (induction of anaesthesia);Intraoperative & postoperative requirement of pain killers & the factors affecting the same (for example, age, sex)Timepoint: From Start of procedure till 1 week of postoperative period;The benefits of a Departmental protocol in reducing the intraoperative & postoperative adverse eventsTimepoint: 24 hours from start of procedure (induction of anaesthesia)

Countries

India

Contacts

Public ContactDr Saptashwa Mitra

Tata Memorial Hospital

sumitrabakshi@yahoo.in02224177058

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026