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Clinical Outcomes of Endoscopic Surgery for Lumbar Spinal Canal Narrowing: A Prospective Study

Clinical Outcome of Monoportal Spine Endoscopy in Lumbar Canal Stenosis: A Prospective Interventional Study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/07/113643
Enrollment
18
Registered
2026-07-07
Start date
Unknown
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Health Condition 1: M480- Spinal stenosis

Interventions

Intervention1: Percutaneous Monoportal Spine Endoscopic Lumbar Decompression: Monoportal Spine Endoscope is a surgical 8-9 MM Rigid Endoscope, Which has a optic channel for Visualization of structure,

Sponsors

Department of Physiotherapy Chhatrapati Sahu Ji Maharaj University
Lead Sponsor
CHHATRAPATI SAHU JI MAHARAJ UNIVERSITY
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: 1. MRI confirmed degenerative lumbar canal stenosis involving central, lateral recess and or foraminal regions 2. Patients with stable grade 1-2 lumbar spodylolisthesis 3. Symptoms refractory to adequate conservative management. 4. Ability to provide informed written consent.

Exclusion criteria

Exclusion criteria: 1. Unstable or high-grade degenerative lumbar spondylolisthesis 2. Lumbar spinal pathology due to tumour, infection, fracture, or deformity 3. Previous lumbar surgery at the index level Pregnancy 4. Severe medical comorbidities contraindicating surgery

Design outcomes

Primary

MeasureTime frame
1. To estimate length of stay (LOS) 2. To estimate Pre and Post intervention, VAS of backpain and VAS of leg pain 3. To estimate Pre and Post intervention, change in disability by ODI scoring 4. To estimate Pre and Post intervention, change in claudication distance by Self-Paced Walk Test 5. To estimate incidence of Reoperation 6. Any complications their incidence Timepoint: 1. To estimate length of stay (LOS) 2. To estimate Pre and Post intervention, VAS of backpain and VAS of leg pain 3. To estimate Pre and Post intervention, change in disability by ODI scoring 4. To estimate Pre and Post intervention, change in claudication distance by Self-Paced Walk Test 5. To estimate incidence of Reoperation 6. Any complications their incidence—

Secondary

MeasureTime frame
1. To estimate Operative time 2. Operators experience 3. Radiographic decompression metrics where available 4. To estimate Operative time 5. Operators experience 6. Radiographic decompression metrics where available 1. To estimate Operative time 2. Operators experience 3. Radiographic decompression metrics where available Timepoint: at day 2,10, 30,90, 180—

Countries

India

Contacts

Public ContactChandra Shekhar Singh

Chhatrapati Sahu Ji Maharaj University

Digvijaysharma@csjmu.ac.in9236072730

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Aug 10, 2026