Bleeding control and improvement of the quality of surgical field in sinus endoscopic surgery of those who need surgery that did not respond to drug therapy.. Chronic sinusitis, unspecified
Conditions
Interventions
Intervention 1: Intervention group: a group of 56 patients with chronic rhinosinusitis, requiring sinus endoscopic surgery was obtained. For preoperation patient , a mesh soaked in a mixture of phenyl
Sponsors
Boushehr University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: Patients with chronic rhinosinusitis that don't not respond to drug therapy and require sinus surgery The age of the participant(s) must be between 18 and 60 years old The amount of hemoglobin of the participant should be above 10 g/dl the amount of Bleeding time (BT), Prothrombin time (PT), Partial thromboplastin time (PTT), International normalized Ratio (INR) should be normal in participants.
Exclusion criteria
Exclusion criteria: Participants with cardiovascular disorders. Participants who have coagulation disorders or who are taking anticoagulant medicines(drugs) Participants with inherited coagulation disorders such as thrombophilia. Participants with coagulation disorders history in the past. Participants who have a history (record) of allergy to any drug(s) in the past. Participants who have been suffering from renal deficiency in the past. Participants with cirrhosis. Participants with chronic diseases, such as diabetes and hypertension. Participants who are pregnant. participants with malignant nasal tumor. Color blindness
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Bleeding during surgery. Timepoint: At 15th, 30th and 45th minute after intervention. Method of measurement: The Boezaart measuring scale.;Surgeon's satisfaction with quality of surgical field. Timepoint: At 15th, 30th and 45th minute after intervention. Method of measurement: Likert scale plan for satisfaction. | — |
Secondary
| Measure | Time frame |
|---|---|
| Blood pressure. Timepoint: every 15 minutes after start of surgery. Method of measurement: heart monitoring.;Bleeding volume. Timepoint: every 15 minutes after start of surgery. Method of measurement: suction device.;Pulse rate. Timepoint: every 15 minutes after start of surgery. Method of measurement: heart monitoring. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactAllahkaram Akhlaghi
Boushehr University of Medical Sciences
Outcome results
None listed