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Effects of alendronate on the postoperative fusion of lumbar in traumatic patients

Efficacy of oral alendronate on lumbar spine Fusion rate after surgery, in traumatic mens 18 to 50 years old

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2013113015588N1
Enrollment
60
Registered
2013-12-20
Start date
2014-01-01
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

lumbar traumatic fracture. Fracture of lumbar vertebra

Interventions

Intervention 1: Oral alendronate 35 mg tablet once a week for six months in the intervention group. Intervention 2: In the control group at six months after the surgical intervention of alendronate or
Treatment - Drugs
Treatment - Other
Oral alendronate 35 mg tablet once a week for six months in the intervention group
In the control group at six months after the surgical intervention of alendronate or placebo was not used

Sponsors

Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria : males with 18 - 50 years old:traumatic fracture in one level of L2-L4:normal neurological exam:Informed consent to participate in research Exclusion criteria : female patients:age less than 18 or more than 50 years :Traumatic fractures of the spine is not involved L2 to L4 or if more than one vertebra is involved:along with the dislocation of spine fractures or severe head trauma associated with such trauma, or severe orthopedic problems exist:lack of consent to participate in this study at any time:nephrolithiasis history or a history of peptic ulcer

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Maintain the level of lumbar lordosis after fusion surgery. Timepoint: Before the intervention and six months after intervention. Method of measurement: Digital radiograpy 4 for AP, Lat, Flex, and Ext.;Pain at the site of spine trauma. Timepoint: Before the intervention and six months after intervention. Method of measurement: Pain Questionnaire.;Extent of bony fusion at the site of surgical intervention. Timepoint: Before surgical intervention, and six months after surgical intervention. Method of measurement: Digital radiograpy 4 for AP, Lat, Flex and Ext.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactReza Pezeshkan.MD

Tabriz University of Medical Sciences

pezeshkan_reza@yahoo.com+98 41 1334 0830

Outcome results

None listed

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