selecting the lowest fused vertebra in patients with Scheuermann's kyphosis

Comparison of two methods in selecting the lowest fused vertebra in patients with Scheuermann's kyphosis based on complications

Status

Recruiting

Phases

Phase 2

Study type

Interventional

Source

IRCT

Registry ID

IRCT20190220042778N1

Enrollment

Registered

2024-01-03

Start date

2024-01-05

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

Scheuermann's Kyphosis. Kyphosis and lordosis

Interventions

Intervention 1: Intervention group: sagittal stable vertebra-In this method, the pedicle screw is placed in the patient s vertebra. This screw is from the Asve company. Intervention 2: Control group:

Eligibility

Sex/Gender

All

Age

8 Years to 25 Years

Inclusion criteria

Inclusion criteria: Scheuermann's kyphosis has been definitively diagnosed by a specialist doctor based on physical examination, radiography and patient history. Patient consent to participate in the study

Exclusion criteria

Exclusion criteria: Having an underlying disease that affects the spine. Having osteoporosis

Design outcomes

Primary

Measure	Time frame
Distal junctional disease. Timepoint: One month, two months and 6 months. Method of measurement: Physical examination and radiography 6 months after surgery.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAli Andalib

Esfahan University of Medical Sciences

ali_andalib@yahoo.com+98 913 317 2522

Outcome results

None listed

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