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Comparison of the Effectiveness of dexmedetomidine and propofol in electrochemotherapy of breast cancer skin lesion

Comparison of dexmedetomidine versus propofol intravenous sedation for electrochemotherapy of breast cancer skin lesion: double-blinded clinical trial

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240515061805N1
Enrollment
36
Registered
2024-05-23
Start date
2024-05-22
Completion date
Unknown
Last updated
2024-05-27

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

Conditions

breast cancer skin lesion. Secondary malignant neoplasm of skin

Interventions

Intervention 1: Intervention group: Propofol injection before electrochemotherapy, with a dose of 25 -75 macro/min/kg in breast cancer patients with skin metastasis who are candidates for electrochemo

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Symptomatic metastatic skin lesions (like bleeding, exudation, smell or ulceration) development of skin metastases, in which the symptoms mentioned can be expected Patients who receive systemic treatment and have a good effect on their primary cancer, but their skin lesions do not respond to these treatments or are progressing patients preferring electrochemistry multiple skin lesions or a lesion larger than 1 cm ASA group II, I, III patients between 18 and 60 years old

Exclusion criteria

Exclusion criteria: Pregnancy and breastfeeding Allergy to any of the drugs used in the study hypertension impaired liver and kidney function Hereditary heart diseases ischemic heart disease, smoking using beta blockers and sedative drugs refusing to sign an informed consent form

Design outcomes

Primary

MeasureTime frame
Assessment of patient recovery time with Aldrete score based on assessment of vital signs and consciousness. Timepoint: after operation. Method of measurement: Aldrete score.;Neuropathic pain scale. Timepoint: before and after operation. Method of measurement: neuropathic pain scale.;Ramsay sedation scale. Timepoint: before, during and after operation. Method of measurement: Ramsay sedation scale.;Bispectral index. Timepoint: during operation. Method of measurement: Bispectral index sensor.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSogol Asgari

Shahid Beheshti University of Medical Sciences

drasgari98429@gmail.com+98 21 5541 9005

Outcome results

None listed

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