Comparison of transpedicular fixation with fusion with transpedicular fixation alone in spondylolisthesis: A Randomized Control Trial

Comparison of Transpedicular fixation with fusion with transpedicular fixation alone in spondylolisthesis

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20230907059376N3

Enrollment

Registered

2023-12-09

Start date

2021-08-21

Completion date

Unknown

Last updated

2024-01-22

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

Conditions

Spondylolisthesis. Spondylolisthesis

Interventions

Intervention 1: Intervention group: Participants randomized to intervention group, undergoing Transpedicular Fixation with Fusion, will receive bilateral transpedicular fixation using pedicle screws,

Eligibility

Sex/Gender

Male

Age

18 Years to 45 Years

Inclusion criteria

Inclusion criteria: First and second grade degenerative lumbar spondylolisthesis patients Patients who would consent to participating in the study under ethical conditions Both Gender Male and Female Age 18-45 years

Exclusion criteria

Exclusion criteria: Patients with additional lumbar spondylolisthesis types Patients with additional lumbar degenerative spondylolisthesis grades (3rd and 4th grades) Patients with additional spine pathology (lumbar fracture, disc prolapse) Patients who respond to conservative treatment

Design outcomes

Primary

Measure	Time frame
Lumbar spine disability. Timepoint: Post-surgery for baseline and then after 6 and 12 months. Method of measurement: Oswestry Disability Index (ODI).;Pain. Timepoint: Post-surgery for baseline and then after 6 and 12 months. Method of measurement: Visual analogue scale (VAS).	—

Countries

Pakistan

Contacts

Public ContactMahboob Khan

Afridi Medical Complex, Peshawar

mehboob509@gmail.com+92 91 5711751

Outcome results

None listed

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