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Evaluation of the effect of tidal Volume on operative blood loss

Evaluation of the effect of Tidal Volume on operative blood loss in patients undergoing posterior spinal fusion in Firozgar hospital during 2012-2013

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2013100111398N4
Enrollment
34
Registered
2013-11-12
Start date
2012-03-20
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

Thoracho-lumbar spine fracture. Fractures involving thorax with lower back and pelvis

Interventions

Intervention 1: In intervention group after giving the prone position to the patients, ventilation with low tidal volume (6 ml/kg) will be used until the end of surgery. Intervention 2: In control gro
In intervention group after giving the prone position to the patients, ventilation with low tidal volume (6 ml/kg) will be used until the end of surgery.
In control group traditional value of tidal volume ( 10 ml/kg) will be used for ventilation during operative period

Sponsors

Research deputy, Iran University of Medical Siences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Patients who candidate for posterior spinal fusion under general anesthesia; Consent to participate in research project; ASA physical status I-II; Age between 18 years old to 60 years old; BMI< 30 Exclusion criteria: Disagreement for participation; ASA physical status more than II; Emergency surgery; History of previous spinal surgery; Respiratory diseases; Coagulopathies; Cardiovascular disease; Hypertension; Kidney or liver disease; Diabetes Mellitus; History of taking drugs such as: beta blockers; Calcium channel blockers; Digoxin; Anticoagulant; Clonidine; Alcohol and drug abuse; Tumor in the site of surgery

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
The volume of blood loss during surgery. Timepoint: End of surgery. Method of measurement: Volume of blood collected in the suction reservoir and bloody sponges.

Secondary

MeasureTime frame
Surgeon satisfaction from operative field. Timepoint: End of operation. Method of measurement: Standard scoring score.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammad Reza Ghodraty MD.

Iran University of Medical Sciences

m-ghodrati@tums.ac.irmrghodrati@yahoo.com+98 21 8894 6762

Outcome results

None listed

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