Skip to content

A Comparative study between cold steel dissection method and coblation method of tonsillectomy.

A comparative study between Cold Steel Dissection method and Coblation method of Tonsillectomy. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/05/086486
Enrollment
80
Registered
2025-05-07
Start date
Unknown
Completion date
Unknown
Last updated
2025-05-26

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

Conditions

Health Condition 1: J351- Hypertrophy of tonsils

Interventions

Intervention1: Coblation Method: In another group of chronic tonsillitis patient - surgical excision of tonsil with Coblation method by using the Coblator. Post operative surgical outcome measures at

Sponsors

Dr Soma Mandal
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patient indicating surgery as per SIGN criteria in any grade of Tonsil with or without adenoid enlargement, with symptoms affecting speech, swallowing, breathing or sleep and having received at least one course of antibiotics. The following are the SIGN criteria for tonsillectomy: 1. Obstructive sleep apnoea 2. Recurrent acute tonsillitis: 3. Quinsy or peritonsillar abscess:

Exclusion criteria

Exclusion criteria: 1. Age less than 5yrs and more than 15yrs. 2. Patients who are unfit for General anaesthesia. 3. Patients not indicated for surgical management of tonsils as per SIGN criteria. 4. Patients with any debilitating systemic disease. 5. Cleft palate. 6. Cranio-facial abnormalities. 7. Unilateral Tonsillar enlargement 8. Tonsillar malignancy 9. Patients not willing to participate in the study.

Design outcomes

Primary

MeasureTime frame
Outcome will be assessed based on the mentioned parameters and study variables. This study will compare the clinical improvement, hearing outcome, time of surgery and post operative taste sensation changes in the two approaches, and may help in guiding choice of approach for future patients.Timepoint: 1 month 2 months 3 months

Secondary

MeasureTime frame
Post operative painTimepoint: 1 month 2 months 3 months;post operative bleedTimepoint: 1 month 2 months 3 months

Countries

India

Contacts

Public ContactDr Soma Mandal

IPGMER and SSKM Hospital

drsomamandal123@gmail.com9830356275

Outcome results

None listed

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