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Comparative Evaluation of Cervical Epidural Adhesiolysis vs. Selective Nerve Root Block in Managing Chronic Pain in Cervical Post-Surgery Syndrome: A Pilot Study

Comparative Evaluation of Cervical Epidural Adhesiolysis and Selective Nerve Root Block in Managing Chronic Pain of Cervical Post-Surgery Syndrome: An Exploratory Pilot Study. - nil

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/01/079751
Enrollment
40
Registered
2025-01-29
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: G30-G32- Other degenerative diseases of the nervous system

Interventions

Intervention1: cervical epidural adhesiolysis: Patients will undergo cervical epidural adhesiolysis using a specialized catheter under fluoroscopic guidance. The procedure involves targeted mechanical

Sponsors

Nil
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Had cervical surgery performed at least one year before enrollment. (cervical pain either persisting despite surgical intervention or appearing after surgical intervention) Had a history of chronic, function-limiting neck and upper extremity pain lasting for at least 6 months following surgery. Pain unresponsive to conservative treatment including medical management, physical therapy, and previous interventions. Average pain score of more than 4 on an 11 point NRS. competent to understand the study protocol. Will be willing to provide voluntary, written informed consent and willing to participate in the assessment of outcome measurements.

Exclusion criteria

Exclusion criteria: Patient refusal Pain for less than 6 months Coagulopathy and/or patients on anticoagulants. Infection at the site of injection. Hypersensitivity to local anesthetic agent. Evidence of severe psychiatric illness. Absence of prior cervical spine surgery. Uncontrolled or unstable opioid use Any conditions that might compromise the interpretation of outcome assessments. Pregnancy or lactation. History of any major comorbid medical conditions, those interfere with recording of study outcomes (neurological disorders, auto-immune diseases), multiple sclerosis, and pregnancy.

Design outcomes

Primary

MeasureTime frame
Pain relief as assessed by Numerical Rating Scale (NRS) on a scale of 1-10 Timepoint: at baseline and 3 months

Secondary

MeasureTime frame
Improvement in functional status as measured by Neck disability index at respective time intervals.Timepoint: baseline, one month & three months;Analgesic usage Procedural complications (if any)Timepoint: baseline

Countries

India

Contacts

Public ContactDR AJIT KUMAR

AIIMS Rishikesh

ajitdr.ajit@gmail.com9910789377

Outcome results

None listed

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