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Lidocaine as anesthetic adjuvant

TO STUDY THE PHARMACOKINETIC AND PHARMACODYNAMIC EFFECTS OF LIDOCAINE INFUSION ON POSTOPERATIVE ANALGESIA WITH RESPECT TO PHARMACOGENETICS

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
IRCT
Registry ID
IRCT20230830059302N1
Enrollment
300
Registered
2023-09-01
Start date
2023-10-02
Completion date
Unknown
Last updated
2023-10-16

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

Conditions

Patient undergoing Elective abdominal cholecystectomy.

Interventions

Intervention group:.

Sponsors

Self Sponsored
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: • Healthy Pakistani individuals between ages 18-60 years undergoing elective abdominal cholecystectomy. • Patients in classes I and II of the American Society of Anesthesiologists (ASA) scale.

Exclusion criteria

Exclusion criteria: • Not of Pakistani origin • Extremes of age • Patients in classes III, IV, V &, and VI of the ASA scale.• Patient with deranged Liver & renal function test (LFT/RFT) • Pre-operative morphine consumption• Patients on medication with immunosuppressive drugs, Non-steroidal anti-inflammatory drugs, or steroids if taking should stop them one week before surgery

Design outcomes

Primary

MeasureTime frame
To prove that lidocaine is a safe anesthetic adjuvant helps in early recovery and decreases the hospital load.by early mobilization. Timepoint: Samples will be taken at 0, 2, 4 & 6 hrs after the surgery. Method of measurement: BP by sphygmomonometer & plasma level of drugs by HPLC, Interleukin levels by ELISA kit, Genotyping by PCR & RFLP.;Analgesia. Timepoint: VAS. Method of measurement: Facial expression, then after 8 hours through verbel questions.

Secondary

MeasureTime frame
Inflammatory markers. Timepoint: IL levels decline earlier. Method of measurement: ELISA Kit.

Countries

Pakistan

Contacts

Public ContactAyesha Afzal

Wah Medical College

dr.ayeshaafzal@hotmail.com+92 301 5218240

Outcome results

None listed

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