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The effect of Goal-directed fluid therapy on intraoperative transfusion rate in spine surgery

The effect of Goal-directed fluid therapy on intraoperative transfusion rate in spine surgery in Golestan Hospital in 1399

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20201014049024N1
Enrollment
60
Registered
2020-11-09
Start date
2020-04-21
Completion date
Unknown
Last updated
2020-11-30

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

Conditions

Patients undergoing spinal surgery due to spinal canal stenosis or other causes.. Spondylosis

Interventions

Intervention 1: Intervention group: For patients in the intervention group, targeted fluid therapy will be performed according to the protocol. Before induction, 4 mg / kg of crystalloid solution (Rin

Sponsors

Ahvaz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: Age 18 to 70 years Candidate for spine surgery No heart, kidney and liver disease Do not take anticoagulants

Exclusion criteria

Exclusion criteria: Patient dissatisfaction, Existence of pulmonary ral and crackle Existence of pleural effusion

Design outcomes

Primary

MeasureTime frame
Number of units of blood required. Timepoint: During surgery. Method of measurement: Number of injected blood bags.;Bleeding rate. Timepoint: During surgery. Method of measurement: Measurement of blood in suction, gas and blood clots.;Incidence of acidosis. Timepoint: During surgery. Method of measurement: Arterial blood gas testing.;Urinary output. Timepoint: During surgery. Method of measurement: The amount of urine in the bladder.;The need for a vasopressor. Timepoint: During surgery. Method of measurement: Number of vasopressor injections.;Need a ventilator after surgery. Timepoint: Immediately after surgery. Method of measurement: Need to use a ventilator after surgery.;Crystalloid requirements during surgery. Timepoint: During surgery. Method of measurement: Injectable serum volume.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSheida Nassajian

Ahvaz University of Medical Sciences

Nassajian.sh@ajums.ac.ir+98 61 3373 8383

Outcome results

None listed

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