Post operative pain relief in tonsilectomy patient after peritonsillar infiltration.

Comparison of the efficacy of Ropivacaine and Ropivacaine with Dexmeditomidine in post tonsilectomy pain relief after peritonsilar infiltration.A prospective randomized double blind study.

Status

Recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2017/10/009983

Enrollment

Registered

2017-10-03

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: null- Pediatric patient of age group 4 to 14 undergoing tonsillectomy.

Interventions

Intervention1: Injection ropivacaine: Ropivacaine is cheap and potent local analgesic with much of sensory blocking activity and which can be infiltrated locally. Intervention2: Injection Dexmeditomid

Eligibility

Inclusion criteria

Inclusion criteria: 1-Age of patient 4-14 years 2-Gender- Male and Female 3-History of chronic tonsillitis for more than 3 month 4-ASA grade 1 and 2

Exclusion criteria

Exclusion criteria: Acute pharyngeal infection Peritonsillar abscess formation Cardiovascular, renal or liver disease Neurological or psychiatric disease Coagulation disturbances

Design outcomes

Primary

Measure	Time frame
Pain assessment using a Visual Analog Scale, marked with 0 mark no pain and 10 worst pain experienced b Childrens Hospital of Eastern Ontario Pain Scale CHEOPS c Wong Baker faces pain rating scale 2 Time to first and subsequent request of supplemental analgesics and total dose of rescue analgesics consumed 24 h postoperative 3 Post operative pain on deglutation o mild 1 moderate and 2 severe Timepoint: by August 2018	—

Measure

Time frame

Pain assessment using a Visual Analog Scale, marked with 0 mark no pain and 10 worst pain experienced b Childrens Hospital of Eastern Ontario Pain Scale CHEOPS c Wong Baker faces pain rating scale 2 Time to first and subsequent request of supplemental analgesics and total dose of rescue analgesics consumed 24 h postoperative 3 Post operative pain on deglutation o mild 1 moderate and 2 severe Timepoint: by August 2018

—

Secondary

Measure	Time frame
1 The amount of bleeding was assessed using a point scale 0 No bleeding 1 mild to moderate bleeding and 2 severe bleeding 2 The childrens families graded their satisfaction regarding analgesia before discharge as follow 1 not satisfied 2 mildly satisfied and 3 very satisfied Timepoint: by August 2018	—

Countries

India

Contacts

Public ContactDr Rahul Singh

Government medical college bhavnagar

trivedi_lopa@yahoo.in9428009958

Outcome results

None listed

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