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Comparing the effectiveness of perineural corticosteroid injection and perineural dextrose prolotherapy for treating occipital neuralgia in patients in a Central Indian tertiary care hospital: A , parallel arm, randomised, non-inferior trial

Comparison of efficacy of perineural dextrose prolotherapy with perineural corticosteroid injection in the treatment of patients with occipital neuralgia in a tertiary care hospital in the Central India: A non-inferior, randomised, assessor blind, parallel arm study - NIL

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/02/081465
Enrollment
50
Registered
2025-02-28
Start date
Unknown
Completion date
Unknown
Last updated
2025-03-03

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

Conditions

Health Condition 1: 3- Administration

Interventions

Intervention1: Perineural dextrose prolotherapy: patients with occipital neuralgia will be given perineural injection of 1 ml 5% dextrose and 1 ml 2% lignocaine around Greater, lesser and/or third occ

Sponsors

Indian Council of Medical Research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Diagnose case of occipital neuralgia according to ICHD 3 criteria A Unilateral or bilateral pain fulfilling criteria B to E B Pain is located in the distribution of the greater, lesser, and/or third occipital nerves C Pain has two of the following three characteristics 1 Recurring in paroxysmal attacks lasting from a few seconds to minutes 2 Severe intensity 3 Shooting, stabbing, or sharp in quality D Pain is associated with both of the following 1 Dysaesthesia and/or allodynia apparent during innocuous stimulation of the scalp and/or hair 2 Either or both of the following a Tenderness over the affected nerve branches b Trigger points at the emergence of the greater occipital nerve or in the area of distribution of C2 E Pain is eased temporarily by local anesthetic block of the affected nerve F Not better accounted for by another ICHD 3 diagnosis

Exclusion criteria

Exclusion criteria: 1 Pregnant females 2 Patients below the age of 18 and above 75 3 Patient with uncontrolled diabetes mellitus 4 Patient on analgesic medication for condition other than occipital neuralgia 5 Patients with neuralgia due to tumor, acute infection and/or trauma

Design outcomes

Primary

MeasureTime frame
pain reduction via VAS score and Barrow Neurological Pain ScaleTimepoint: 1) pre procedure 2) 2 weeks post procedure 3) 4 weeks post procedure 4) 8 weeks post procedure

Secondary

MeasureTime frame
Difference in quality of life as measure by SF-12 scaleTimepoint: 1) pre procedure 2) 2 weeks post procedure 3) 4 weeks post procedure 4) 8 weeks post procedure;ii) To study the efficacy of perineural dextrose prolotherapy and perineural steroid injection in the treatment of patient with occipital neuralgiaTimepoint: 1) pre procedure 2) 2 weeks post procedure 3) 4 weeks post procedure 4) 8 weeks post procedure;To study the dermatomal distribution of occipital neuralgia in Greater Occipital Nerve, Lesser occipital Nerve and third occipital NerveTimepoint: ;Document characteristic of background pain (quality, location, and intensity) and pain exacerbations (frequency, duration, quality) in occipital neuralgiaTimepoint:

Countries

India

Contacts

Public ContactDr Sonali Sahani

AIIMS, Nagpur

harshanand.popalwar@gmail.com9424917696

Outcome results

None listed

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