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comparison of hemodynamic parameters during pneumoperitoneum,post operative pain control in three groups placebo group, lignocaine group ,dexmedetomidine group

To compare the attenuation of hemodynamic response to pneumoperitoneum during laparoscopic cholecystectomy between lignocaine and dexmedetomidine - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/09/057625
Enrollment
144
Registered
2023-09-14
Start date
Unknown
Completion date
Unknown
Last updated
2023-09-18

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

Conditions

Health Condition 1: K00-K95- Diseases of the digestive system

Interventions

Intervention1: LIGNOCAINE ,DEXMEDETOMIDINE: comparison of hemodynamic parameters during pneumoperitoneum,post operative pain control in three groups placebo group, lignocaine group ,dexmedetomidine g

Sponsors

Vydehi institute of medical sciences and research centre
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1)ASA 1-2 2)PATIENTS UNDERGOING ELECTIVE LAPAROSCOPIC CHOLECYSTECTOMY

Exclusion criteria

Exclusion criteria: 1)PATIENT REFUSAL 2)ALLERGY TO LOCAL ANAESTHETIC AGENTS 3)PREGNANT AND LACTATING WOMEN

Design outcomes

Primary

MeasureTime frame
to assess the efficacy of lignocaine & dexmedetomidine in altering hemodynamic response during pneumoperitoneumTimepoint: before induction , before pneumoperitoneum, every 5 minutes during pneumoperitoneum for 30 minutes then half hourly till deflation,after extubation ,in recovery room postop 4 hrs,8 hrs,12 hrs, 24 hrs—

Secondary

MeasureTime frame
comparing the time of request for first postoperative analgesia, sedationTimepoint: ramsay sedation score immediate post op vas score every 4 hours for 24 hours request for first postoperative analgesia—

Countries

India

Contacts

Public ContactDr Radhika Dhanpal

Vydehi institute of medical sciences and research centre

radhika5276@vimsmail.com8049069000

Outcome results

None listed

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