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Comparison of two drugs, Lignocaine and Ketamine intravenous infusion in management of difficult cancer pain

Comparison of Ketamine Vs Lignocaine intravenous infusion in refractory cancer pain - NIL

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/10/058966
Enrollment
66
Registered
2023-10-20
Start date
Unknown
Completion date
Unknown
Last updated
2024-08-19

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

Conditions

Health Condition 1: C00-D49- Neoplasms

Interventions

Intervention1: Lignocaine: Inj Lignocaine 2mg/kg/hr over 6hrs 2 infusions with 12hrs apart-FOLLOW UP for 6weeks Control Intervention1: Ketamine: Inj Ketamine 0.3mg/kg/hr over 6hrs 2 infusions with 12

Sponsors

Basavatarakam Indo American Cancer Hospital and Research Institute, Hyderabad
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients with Refractory cancer pain with NRS >6-7/10 despite optimal opioid drugs (OME >300 mg / day) Patients with refractory neuropathic/mixed pain Patients with life span >8weeks

Exclusion criteria

Exclusion criteria: H/O psychosis Any liver, kidney and heart abnormalities Patients with altered cognitive function H/O drugs hypersensitivity Patients not giving consent

Design outcomes

Primary

MeasureTime frame
Comparison of Ketamine Vs Lignocaine intravenous infusion in refractory cancer pain in reducing severity of pain atleast by 50%Timepoint: 1 year

Secondary

MeasureTime frame
1.Comparison of side effect profile & tolerability of both drugs 2.Comparison of time interval in both drugs till next relapse of acute pain crisisTimepoint: 1 year

Countries

India

Contacts

Public ContactPulluri Sai Sowmya

Baswatarakam Indo American cancer Hospital and research Institute

drprawin78@gmail.com9959893915

Outcome results

None listed

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