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Comparative Study of local pain relief with 4% Lignocaine and Intravenous Tramadol for postoperative pain after removal of tonsils

Clinical Comparative Study of Analgesia with 4% Lignocaine and Intravenous Tramadol for Post-Operative Analgesia after Tonsillectomy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/01/022602
Enrollment
60
Registered
2020-01-03
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: J399- Disease of upper respiratory tract, unspecified

Interventions

Intervention1: Tramadol: Intravenous Tramadol 1mg/kg is given Control Intervention1: Tramadol: Intravenous Tramadol 1mg/kg is given. Control Intervention2: Lignocaine: 4% Lignocaine- a gauze measuring

Sponsors

Dr Sarala H S
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA I & II for elective tonsillectomy

Exclusion criteria

Exclusion criteria: Those who are hypersensitive to lignocaine. Signs of acute pharyngeal infection - Adeno tonsillitis, Peritonsillitis, Peritonsillar abscess. Suspected Malignant Neoplasm. Those who are pregnant and lactating mothers.

Design outcomes

Primary

MeasureTime frame
Postoperative Analgesia Timepoint: Pain assessed at intervals of 30 mins for 4 hrs and 4th hourly for 24 hrs postoperatively by visual analogue scale.—

Secondary

MeasureTime frame
Postoperative nauseaTimepoint: The time to first oral water and solid food intake and incidence rates of nausea are evaluated at intervals of half an hourly for first 2nd hourly, hourly for next 4 hours.—

Countries

India

Contacts

Public ContactSarala H S

Kempegowda Institute Of Medical Sciences

narendrababuchanappa@gmail.com9900214064

Outcome results

None listed

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