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Interventional Management of Trigeminal Neuralgia

Comparison of Percutaneous Radiofrequency Thermocoagulation and Percutaneous Microballoon Compression of Gasserian ganglion in Treatment of Trigeminal neuralgia- A randomized controlled trial.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/01/011494
Enrollment
30
Registered
2018-01-23
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- ASA I and II patients with unilateral trigeminal neuralgia

Interventions

Intervention1: Comparison of Percutaneous Radiofrequency Thermocoagulation and Percutaneous Microballoon Compression of Gasserian ganglion in Treatment of Trigeminal neuralgia: Both the procedure woul

Sponsors

AIIMS New Delhi
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: •Thirty adult patients of either sex diagnosed to have Classical trigeminal neuralgia will be recruited for this study. Classic TN will be diagnosed according to the International Classification of Headache Disorders-II (2004) Classical TN of more than six monthsâ?? duration Pain rating (during the attack) of at least six on a Visual analogue scale (VAS/NRS) No satisfactory pain relief with medical treatment for more than three months; and/or intolerable side effects using oral medications

Exclusion criteria

Exclusion criteria: 1. Patientâ??s refusal to involve in the study 2. History of allergy to drugs used in the procedures 3. Coagulopathy 4. Morbid obesity

Design outcomes

Primary

MeasureTime frame
Multi-dimensional outcomes as recommended by IMMPACT (Initiative on methods, measurement, and pain assessment in clinical trials) The following domains were assessed Pain: by 11point (0-10) NRS Physical functioning: by Brief Pain Inventory-Facial scale Emotional functioning: by Beck Depression Inventory Global improvement: by Patient Global Impression of change Timepoint: Immediate post operative period Day 7 Then every month till 1 year

Secondary

MeasureTime frame
Health related quality of life would be measured by EQ-5D-3L (paper version) questionnaire Spontaneous reporting of symptoms and adverse events with open ended prompts with each visit Complications to be noted: Residual Pain Dysaesthesia Decreased corneal sensation Masseter weakness Diplopia and Procedure related complications:Timepoint: Immediate post op at day 7 then every month for 1 year

Countries

India

Contacts

Public ContactVirender Kumar Mohan

AIIMS New Delhi

dr_vkmohan@yahoo.com

Outcome results

None listed

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