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Surgical Outcome by Scrophy Pedicle in Spondylolisthesis Patients with and Without Modified Changes

Surgical Outcome by Scrophy Pedicle in Spondylolisthesis Patients with and Without Modified Changes

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20120527009878N10
Enrollment
80
Registered
2019-07-31
Start date
2019-08-21
Completion date
Unknown
Last updated
2019-10-07

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

Conditions

Spondylolisthesis patients. Spondylolisthesis

Interventions

Intervention 1: Intervention group: Patients with modiform changes that fall under the fusion with a pedicle screw. Intervention 2: Control group: Patients without modicidal changes under the fusion w

Sponsors

Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: All patients who have a back pain and will be screened for spondylolisthesis.

Exclusion criteria

Exclusion criteria: Patient dissatisfaction

Design outcomes

Primary

MeasureTime frame
Postoperative pain in patients with and without changes in the mood. Timepoint: 6 to 12 months after surgery. Method of measurement: In follow-up, the pain of postoperative patients will be measured by strip tapeworm. The displacement and fracture of the screw will be evaluated by the postoperative control graph and the presence of infection or its absence with serial examinations will be evaluated every three to six months.—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Moslem Shakeri

Tabriz University of Medical Sciences

shakerim@gmail.com+98 44 1333 8507

Outcome results

None listed

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