Fibrinogen effect on bleeding rates in surgeries

Phase 3

Recruiting

• Conditions: umbar discopathy.; Lumbar and other intervertebral disc disorders with radiculopathy

• Registration Number: IRCT20180811040763N1
• Lead Sponsor: Ahvaz University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 11 September 2018

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 28

Inclusion Criteria

Patients candidate of lumbar surgery
Age range: 18 to 60 years old

Exclusion Criteria

Patients with cardiovascular diseases
Patients with anemia or bleeding disorders
Consumption of anticoagulant medications
History of spinal surgery

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Serum fibrinogen level. Timepoint: Before anesthesia induction (pre-intervention), immediately, 6 and 24 hours after the completion of the surgical operation. Method of measurement: Blood test.;Partial Thromboplastin Time (PTT). Timepoint: Before anesthesia induction (pre-intervention), immediately, 6 and 24 hours after the completion of the surgical operation. Method of measurement: Blood test.;Prothrombin Time (PT). Timepoint: Before anesthesia induction (pre-intervention), immediately, 6 and 24 hours after the completion of the surgical operation. Method of measurement: Blood test.;Hematocrit (HCT). Timepoint: Before anesthesia induction (pre-intervention), immediately, 6 and 24 hours after the completion of the surgical operation. Method of measurement: Blood test.;Hemoglobin (HB). Timepoint: Before anesthesia induction (pre-intervention), immediately, 6 and 24 hours after the completion of the surgical operation. Method of measurement: Blood test.