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A clinical trial to study efficacy and safety of pulsed radiofrequency as treatment of oral cancer pain.

Efficacy of pulsed radiofrequency ablation for the treatment of oarl cancer pain involving glossopharyngeal nerve.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2016/08/007179
Enrollment
30
Registered
2016-08-12
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- Cancer pain involving glossopharyngeal nerve in a case of oropharyngeal carcinoma with no curative intervention planned

Interventions

Intervention1: Pulsed Radiofrequency Ablation: Pulsed Radiofrequency Ablation of the Glossopharyngeal nerve causing pain will be performed once under sedation in operation theater Control Interventio

Sponsors

Post Graduate Institute of Medical Education Research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Adult population (18-65 years)suffering from oropharyngeal carcinoma with no curative intervention planned( not fit for surgery) undergoing treatment by WHO step ladder II method still complaining of severe pain ( NRS >5) in the base of tongue, tonsillar fossa, pharynx- area mainly supplied by glossopharyngeal nerve.

Exclusion criteria

Exclusion criteria: unstable cardio-respiratory disorder coagulation & hematological disorder psychological disorder & history drug abuse non compliant for 3 months follow up injection site not suitable due to presence of infection , lymph node enlaegement bilateral involvement of glossopharyngeal nerve

Design outcomes

Primary

MeasureTime frame
Efficacy of PRF ablation of glossopharyngeal nerve for the treatment of cancer pain by pain score by numerical rating scale Timepoint: Post intervention - 1week, 2 week, 1 month, 2 month, 3 month

Secondary

MeasureTime frame
Safety profile of PRF of glossopharyngeal nerve in cancer painTimepoint: during & post intervention (120 mins ) & post intervention 1 week, 2 week, 1 month, 2 month,3 month

Countries

India

Contacts

Public ContactDr Suryabrata Chattopadhyay

PGIMER, Chandigarh

bhartineerja@yahoo.com09915575145

Outcome results

None listed

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