Skip to content

Effect of Intravenous Lignocaine, Peri-tumoral Lignocaine or Standard Care on Biomarkers in Breast Cancer Surgery Patients

Effect of Intravenous Lignocaine, Peri-tumoral Lignocaine or Standard Care on Pro-metastatic Biomarkers in Breast Cancer Surgery Patients: A Triple-arm Randomized Controlled Trial - NIL

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/03/081983
Enrollment
105
Registered
2025-03-07
Start date
Unknown
Completion date
Unknown
Last updated
2026-09-14

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Intravenous Lignocaine: Intravenous lignocaine in a dose of 1.5 mg/kg bolus over 10 minutes prior to induction of anesthesia followed by 2.0 mg/kg/hour until skin closure using a progra

Sponsors

Dr Zainab Ahmad
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA physical status I- to II, with operable breast cancer Stage I to III

Exclusion criteria

Exclusion criteria: Metastatic or recurrent breast cancer, significant comorbidities, contraindications to lignocaine, pregnancy, weight less than 40 kg, preoperative hypotension, immune disorders, or long-term immunosuppressive drug use.

Design outcomes

Primary

MeasureTime frame
Serum levels NETosis biomarkers - H3CitTimepoint: Baseline and at 24 hours after surgery

Secondary

MeasureTime frame
Early cancer recurrenceTimepoint: 2 years or until the end of the study;Angiogenesis Biomarkers - MMP 3, VEGFTimepoint: baseline and at 24 hours after surgery.;Changes in arrays of metabolomic profile and hypoxia inducible factors (HIF)Timepoint: baseline and at 24 hours after surgery.;Serum MPO levelsTimepoint: baseline & 24 hours after surgery

Countries

India

Contacts

Public ContactDr Jagat Kanwar

All India Institute of Medical Sciences (AIIMS), Bhopal

zainaba.anesth@aiimsbhopal.edu.in8860048951

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Sep 19, 2026