Skip to content

Comparision of success rate of treatment between incision and curettage versus incision and curettage with triamcinolone injection for chalazia

Incision and curettage alone versus incision and curettage with perilesional triamcinolone acetonide injection for primary chalazia: A Randomised Controlled Trial

Status
Active, not recruiting
Phases
Phase 3Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/05/014281
Enrollment
106
Registered
2018-05-31
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- Chalazion

Interventions

Intervention1: I & C WITH PERILESIONAL TRIAMCINOLONE INJECTION: Cases were operated using Incision and Curettage . at the time of surgery peri lesional triamcinolone was injected Control Intervention1

Sponsors

Dr Shashi Vashisht
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Lid swelling which is clinically diagnosed as chalazion- a) Of at least one month duration b) Size >3 mm c) Not responding to conservative management for a minimum of 2 weeks. A lesion would be categorized clinically as chalazion based on the following diagnostic features: Firm painless swelling in either lid involving the tarsal plate, increasing gradually in size with no symptoms of inflammation. 2. Subject able and willing to participate in the study.

Exclusion criteria

Exclusion criteria: 1. Subject on anticoagulant which cannot be discontinued. 2. Ocular and periocular infection within 14 days prior to surgery. 3. Pregnant and breast feeding women. 4. Patient with known allergy to xylocaine or triamcinolone acetonide used in the study.

Design outcomes

Primary

MeasureTime frame
Lesion resolution measuring greater than 80%. Timepoint: Two weeks

Secondary

MeasureTime frame
1. Period required for resolution of lesion. 2. Period required for resolution of inflammation. 3. Complications 4. Inflammation score at each visit. Timepoint: 1.Two weeks 2.Two weeks 3.Two weeks 4.Two weeks

Countries

India

Contacts

Public ContactDr Niharika

PGIMER Dr RMLHospital

tarudewan@hotmail.com9810673180

Outcome results

None listed

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