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The study is a comparative study between intravenous Lignocaine with intravenous Lignocaine and magnesium sulphate combination for laparoscopic Nephrectomy to evaluate the effectiveness of pain management during post operative in 24 hours

Comparison of intravenous Lignocaine with intravenous Lignocaine and Magnesium sulphate combination for laparoscopic Nephrectomy

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
CTRI
Registry ID
CTRI/2022/03/041115
Enrollment
100
Registered
2022-03-15
Start date
Unknown
Completion date
Unknown
Last updated
2022-04-04

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

Conditions

None listed

Interventions

Control Intervention1: NIL: NIL

Sponsors

Indhira gandhi institue of medical sciencePatna
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Elective laparoscopic Nephrectomy

Exclusion criteria

Exclusion criteria: 1 Refused consent, 2 Allergic to local anaesthetic agent and opiods 3 on long term analgesic to chronic pain 4 Impaired liver function 5 Has a history of arrhythmia 6 Viral marker reactive 7 Covid 19 positive.

Design outcomes

Primary

MeasureTime frame
quality of recovery scoreTimepoint: at 24 hr postoperative period

Secondary

MeasureTime frame
hemodynamics every 30 min after starting infusion. NRS pain score total opioid consumptionTimepoint: 24 hrs postoperative period

Countries

India

Contacts

Public ContactSwati

Indira Gandhi Institute of Medical Science,Patna,Bihar.

nokzei22@yahoo.com8731955881

Outcome results

None listed

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