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Percutaneous Adhesiolysis in Failed Back Surgery Syndrome(FBSS)

Comparative study in Percutaneous Adhesiolysis with isotonic saline vs hypertonic saline in management of Failed Back Surgery Syndrome - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/11/076755
Enrollment
72
Registered
2024-11-13
Start date
Unknown
Completion date
Unknown
Last updated
2024-12-09

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Percutaneous adhesiolysis with hypertonic saline: Percutaneous adhesiolysis of the epidural adhesions done under C-arm guidance with methyl prednisolone, local anesthetic, hyaluronidase

Sponsors

Harivignesh
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Pt should have undergone spinal procedure for Low back pain which is atleast 6 months back, presented with low back pain or radicular pain or both with VAS of more than or equal to 6. MRI showing post-procedure changes or Presence of contrast filling defect in epidurogram. Failed conservative management post-intervention which includes physical therapy, pharmacotherapy and modalities

Exclusion criteria

Exclusion criteria: 1.Low back pain due to facet joint or sacro-iliac joint pathologies 2.Inflammatory low back pain 3.Uncontrolled medical illness 4.Uncontrolled psychiatric illness 5.Any other conditions interfering with the study results 6.Allergic to lignocaine or steroids 7.Coagulopathy 8.Presence of red flag signs (Recent trauma, Fever, new onset neurological deficit, malignancy, fracture) 9.Patient refusal

Design outcomes

Primary

MeasureTime frame
Decrease in pain(by VAS) and improvement in disability(by Oswestry Disability Index)Timepoint: baseline, 2 weeks, 4 weeks and 12 weeks

Secondary

MeasureTime frame
need of analgesics, need to modalities in control of painTimepoint: pre-procedure, 2 weeks, 4 weeks, 12 weeks.

Countries

India

Contacts

Public ContactProf Dr Rajesh Pramanik

IPGME&R and SSKM hospital

rpramanik2000@yahoo.com9432594882

Outcome results

None listed

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