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Effects of plasmapheresis on patients with unstable complex pelvic fracture and long bones

Effects of plasmapheresis on respiratory condition and acidosis of patients with unstable complex pelvic fracture and long bones

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014082718946N1
Enrollment
12
Registered
2014-10-03
Start date
2014-10-01
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

Unstable complex fracture of pelvic or long bones..

Interventions

Intervention group: Patients with unstable complex fracture of hip and long bones, who are admitted to intense care unit, will be examined to assess their respiratory status (Arterial blood gas, respi
Treatment - Devices

Sponsors

Vice chancellor for research, Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: age between 15 and 65 years old; having unstable complex hip or long bone fracture; being admitted to Intense care unit; being tachypneic; suffering respiratory distress; having low oxygen saturation; having Acidosis. Exclusion criteria: having renal failure history; Glascow coma score less than 8 at time of hospitalization; having angioplasty history; having history of chronic respiratory disease (e.g. Asthma, chronic obstructive pulmonary disease,...); concomitant renal, hepatic, cardiac or central nervous system injury in recent trauma; unstable hemodynamic; requiring surgical intervention.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Respiratory rate. Timepoint: Daily and 2 hours after intervention. Method of measurement: Counting by physician.;Respiratory distress. Timepoint: Daily and 2 hours after intervention. Method of measurement: Examination by physician.

Secondary

MeasureTime frame
Arterial blood gas. Timepoint: Daily and 2 hours after intervention. Method of measurement: Arterial blood gases laboratory.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Ramin Azhough

Emam Reza educational-medical center

ali.shahavand92@yahoo.com+98 41 3334 1317

Outcome results

None listed

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