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Assess the benefit of Anaesthetizing Superior Cluneal Nerve in Low back pain

Evaluation of the Efficacy of Superior Cluneal Nerve Block in Low Back Pain: A Prospective Observational Study - SCNB

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2017/05/008670
Enrollment
25
Registered
2017-05-26
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- Patients with pain over the iliac crest and buttock accompanied by a trigger point over the posterior iliac crest 7-8 cm from the midline

Interventions

Intervention1: Superior Cluneal Nerve Block: The Superior Cluneal Nerve Block will be done in OT under fluoroscopic guidance. Patient will be positioned prone and iliac crest identified in antero-post
a marker is placed over the iliac crest 7cm from the L5 spinous process. A 25G 10 cm needle will be inserted in end on fashion towards the iliac crest and 2ml 1% lidocaine will be injected after hitti

Sponsors

Sanjay Gandhi Postgraduate Institute of Medical Sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients in the age group of 18-60 years with complaint of unilateral low back pain over the iliac crest and buttock for more than 6 months not responding to conservative measures

Exclusion criteria

Exclusion criteria: Patients who have undergone spine surgery Patients with vertebral fracture Patients with infectious diseases of spine Patients with radicular symptoms Patients with uncontrolled psychiatric ailments Patients with uncontrolled medical diseases Patients with spine malignancy Patients with coagulopathy Patients with infection at the local site Patient refusal.

Design outcomes

Primary

MeasureTime frame
Severity of pain before and after Superior Cluneal Nerve BlockTimepoint: Baseline (pre-procedure) and 2 weeks, 1, 3 and 6 months post-procedure

Secondary

MeasureTime frame
Patientâ??s functional status assessment by using Oswestry Disability IndexTimepoint: Baseline (pre-procedure) and 2 weeks, 1, 3 and 6 months post-procedure;Percentage pain relief (â?¥ 50% taken as significant pain relief)Timepoint: Baseline (pre-procedure) and 2 weeks, 1, 3 and 6 months post-procedure;Psychological assessment of patient by using DSM-IV scaleTimepoint: Baseline (pre-procedure) and 2 weeks, 1, 3 and 6 months post-procedure;Reduction of analgesic usageTimepoint: Baseline (pre-procedure) and 2 weeks, 1, 3 and 6 months post-procedure

Countries

India

Contacts

Public ContactSujeet Kumar Singh Gautam

Sanjay Gandhi Post-graduate Institute of Medical Sciences

docsksg@gmail.com8765974046

Outcome results

None listed

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