Skip to content

Role of pain block in chronic facial pain

Comparative evaluation of superior cervical plexus block with sham block in cervical pain syndrome due to degenerative cervical spine: A randomized controlled trial.

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/12/022491
Enrollment
20
Registered
2019-12-23
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: G542- Cervical root disorders, not elsewhere classified

Interventions

Intervention1: Group II: patients will receive ultrasound guided 8 ml 0.2% ropivacaine and 4 mg dexamethasone in superficial cervical plexus block. Control Intervention1: Group I: patients will recei

Sponsors

Department of Anaesthesia and Intensive Care
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. 18-75 years of age 2. Either sex 3. Pain at angle of mandible, facial, pre or post auricular area, anterior neck, pain in throat (cervical spine syndrome) for more than 3 months inspite of medical management of chronic pain with incidental degenerative changes in cervical spine . 4. Patients willing for the SCPB block or sham.

Exclusion criteria

Exclusion criteria: 1. Patient with red flag conditions, such as malignancy, infection, metabolic phenomena, severe trauma and associated symptoms such as recent onset, fever, weight loss, and night sweats. 2. Sensory and motor weakness 3. Coagulopathy 4. Infections at procedural site 5. Difficulty in breathing due to involvement of diaphragm. 6. Severe systemic disease. 7. Un-cooperative patient

Design outcomes

Primary

MeasureTime frame
1. Pain recorded on visual analogue scale Timepoint: 1. Before the block, after 20 minutes of the blocks and thereafter on monthly intervals till three months

Secondary

MeasureTime frame
Any reduction in analgesic drugs Heamodynamics quality of life score adverse effectsTimepoint: every month till three months before the block, after 20 minutes of the blocks and thereafter on monthly intervals till three months. every month till three months after 15 minutes of the blocks and thereafter on monthly intervals till three months.

Countries

India

Contacts

Public ContactVanita Ahuja

Government Medical College and Hospital

dpkthapa@gmail.com09646121524

Outcome results

None listed

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