Effects of three anesthetics on intraoperative bleeding and postoperative pai
Phase 2
Recruiting
- Conditions
- nasal fracture.Fracture of nasal bones
- Registration Number
- IRCT20170316033099N1
- Lead Sponsor
- Birjand University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 108
Inclusion Criteria
Signing informed consent
age between 6 and 50 years
nasal fracture
Exclusion Criteria
Pregnancy and breastfeeding
Bladder disease
Known allergic reactions to antihistamines, benzodiazepines, or topical anesthetics
Open nasal fracture reduction or concurrent surgery on the nose septum
Any coagulation disorder or excessive pain
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Postoperative pain. Timepoint: 0, 6, and 24 hours after the operation. Method of measurement: Visual analog scale.;The amount of intraoperative blood loss. Timepoint: After operation. Method of measurement: The amount of blood suctioned; the number of gauzes and long gauzes used; the amount of blood in the surgery field, on the surgery drape, and in the drain.
- Secondary Outcome Measures
Name Time Method Systolic and diastolic blood pressure. Timepoint: At admission, two times during the operation, one time before the patient leaves the recovery room. Method of measurement: sphygmomanometer and monitoring device (Sa'adat Company).;Heart rate. Timepoint: before and after the operation. Method of measurement: monitoring device (Sa'adat Company).;Hemoglobin and hematocrit levels. Timepoint: before and after surgery. Method of measurement: laboratory.