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Assessment of post operative pain relief in tonsillectomy surgery using two different local anesthetics

ASSESSMENT OF POSTOPERATIVE ANALGESIC EFFECT BY INFILTRATION OF BUPIVACAINE AND ROPIVACAINE IN THE ANTERIOR PILLARS OF TONSILS - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2024/02/062790
Enrollment
46
Registered
2024-02-19
Start date
Unknown
Completion date
Unknown
Last updated
2025-09-15

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Infiltration of 0.2% Ropivacaine in Group B: Patients posted for tonsillectomy will be taken as Group A and B Group B children will receive 2ml of 0.2% Ropivacaine by Injection Aspirat

Sponsors

Sree Balaji Medical College and Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA I AND II WEIGHT MORE THAN 10KILOGRAMS

Exclusion criteria

Exclusion criteria: ASA III AND ABOVE ALLERGIC REACTIONS SIGNS OF ACUTE PHARNYGEAL INFECTIONS PERITONSILLAR ABSCESS PARENTS NOT WILLING BLEEDING DISORDER USE OF REGULAR ANALGESIC MEDICATION

Design outcomes

Primary

MeasureTime frame
post operative pain relief for surgical procedure tonsillectomyTimepoint: After Administration of local anesthetics postoperatively 15mins 30 mins 1 hr every 1hr upto 6hrs—

Secondary

MeasureTime frame
to assess the requirement for rescue anlgesiaTimepoint: After Administration of local anesthetic postoperatively 15mins 30 mins 1 hr every 1hr upto 6hrs—

Countries

India

Contacts

Public ContactKala B

Sree Balaji Medical College and Hospital

kalamhn@gmail.com9444680908

Outcome results

None listed

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