Evaluation of the effects of surgicel in open prostatectomy surgery
Not Applicable
Recruiting
- Conditions
- Open prostatectomy.
- Registration Number
- IRCT20200219046557N1
- Lead Sponsor
- Tabriz University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Male
- Target Recruitment
- 30
Inclusion Criteria
Patient who are candidates for open prostatectomy
Patients aged 40 to 90 years
Having informed consent to participate in the study
Exclusion Criteria
Existence of an bleeding disorder
History of previous prostatic or urethral surgery; (c)
Having bladder stone.
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Hemoglobin level. Timepoint: Preoperative, postoperative, days 2 and 3. Method of measurement: According to the lab and on the basis grams per deciliter.;Intraoperative blood loss. Timepoint: At the end of surgery. Method of measurement: The volume of blood absorbed by surgical gauze was estimated using Gauze Visual Analogue method. The mentioned figures plus the amount of blood in the surgical suction pump was considered as the total amount of intraoperative blood loss.;Hematocrit. Timepoint: Preoperative, postoperative, days 2 and 3. Method of measurement: According to the lab and on the basis percent.
- Secondary Outcome Measures
Name Time Method Infection. Timepoint: 7 days after surgery. Method of measurement: Redness,secretion, tenderness in the wound or wound dehiscence.