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A Randomised Controlled Trial to compare two surgical techniques (OLIF and MIS TLIF) for correcting lumbar spondylolisthesis

Comparision between Oblique lumbar interbody fusion (OLIF) and MIS TLIF for lumbar spondylolisthesis : A randomised controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/08/015233
Enrollment
56
Registered
2018-08-08
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- 1 Patients with symptomatic lumbar spondylolisthesis not improving on 6 months of conservative management 2 Age- 18-60 years 3 Single level listhesis 4 Grade I or II listhesis Health Condition 2: M488- Other specified spondylopathies Health Condition 3: M992- Subluxation stenosis of neural canal Health Condition 4: M992- Subluxation stenosis of neural canal

Interventions

Intervention1: Minimal Invasive Transforaminal Lumbar Interbody Fusion (MIS TLIF): Paramedian skin incisions will be placed 1- 2cm lateral to pedicles. Jamshidi needles will be placed at pedicle screw

Sponsors

Dr V V Ramesh Chandra
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1 Patients with symptomatic lumbar spondylolisthesis not improving on 6 months of conservative management 2 Patient age between 18-60 years 3 Single level listhesis 4 Grade I or II listhesis as per Meyerding classification

Exclusion criteria

Exclusion criteria: 1 Patients with osteoporosis/ Trauma. 2 Patients with high grade listhesis (III, IV). 3 Spondylolisthesis at L5-S1 level 4 Patients who are medically unfit for surgery. 5 Previous surgery at proposed treatment level. 6 Patients not consenting for surgery 7 Multiple level listhesis

Design outcomes

Primary

MeasureTime frame
The intraoperative blood loss, Duration of the procedure, Amount of radiation exposure will be compared. CPK-MB ( Creatine Phospho Kinase - MB) and CRP ( C Reactive Protein) levels to know the iatrogenic muscle injury Post-operative MRI scan to know the multifidus atrophy. Analgesic dependence in terms days of requirement of analgesics. Fusion grading will be assesedTimepoint: First and Sixth month postoperatively

Secondary

MeasureTime frame
Visual Analogue Score (VAS) and Oswestry Disability Index (ODI)Timepoint: First and Sixth month postoperatively

Countries

India

Contacts

Public ContactDr Goutham Hanu T

Sri Venkateswara Institute of Medical Sciences

gouthamhanu1989@gmail.com8861094114

Outcome results

None listed

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