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Pulsed radiofrequency Of Cervical nerves for Managing Post Amputation pain or phantom limb pain

Pulsed radiofrequency adjacent to Cervical Dorsal Root ganglion for refractory phantom limb pain: An Interventional study - NIL

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/07/091014
Enrollment
25
Registered
2025-07-16
Start date
Unknown
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

Health Condition 1: G546- Phantom limb syndrome with pain

Interventions

Intervention1: Pulsed Radiofrequency Ablation (PRFA) near Cervical Dorsal Root Ganglion: Following informed written consent under fluoroscopic guidance Radiofrequency cannula (22G , 100 mm) will be pl

Sponsors

All India Institute of Medical Sciences Rishikesh
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: The patients aged between 18 to 65 years who have undergone upper limb amputation and presently suffering from phantom limb pain will be included in the study. These patients will undergo Pulsed radiofrequency ablation of Cervical Dorsal root ganglion and follow up period will be done at 3 month following the procedure in terms of pain reduction and improvement in quality of life.

Exclusion criteria

Exclusion criteria: Age less than 18 years and more than 65 years Allergy to local Anesthetics Deranged coagulation profile Both upper and lower limb amputee.

Design outcomes

Primary

MeasureTime frame
To Determine the effects of Pulsed Radiofrequency ablation on cervical Dorsal root ganglion with Phantom limb pain in terms of pain relief as assessed by Numerical rating scale . Timepoint: Pain Reduction will be assessed at baseline at 1 month and at 3 months following procedure.

Secondary

MeasureTime frame
To quantify medication regimen using Medication Quantification Scale Timepoint: At 3 months;to Measure patients health status Global Perceived effect using 7 point Likert scale. Timepoint: at 3 months;Emotional functioning of these patients using Hospital anxiety and depression scale (HADS). Timepoint: At 3 months Interval

Countries

India

Contacts

Public ContactRavi Shankar Sharma

AIIMS , Rishikesh

drravishankarsharma4u@gmail.com9993116929

Outcome results

None listed

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