Benign prostatic hyperplasia. Enlarged prostate
Conditions
Interventions
Intervention 1: Intervention group P: Use of Pfannenstiel incision for simple open prostatectomy patients surgery-In this group, the Pfannenstiel skin incision, which is a lower transverse abdominal i
Sponsors
Hamedan University of Medical Sciences
Eligibility
Sex/Gender
Male
Inclusion criteria
Inclusion criteria: Ability to communicate with the researcher Absence of an underlying disease disrupting the research results, such as immune system diseases or coagulation disorders Not taking immunosuppressive drugs Absence of psychological diseases
Exclusion criteria
Exclusion criteria: Unwillingness to participate in the study Failure to sign informed consent Taking opioid drugs or substances
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Time of surgery. Timepoint: During surgery. Method of measurement: By using an electronic timer, the operation time is measured so that when the skin incision is started, the surgeon gives the order (start) and the researcher starts measuring the time, and after the last skin suture is applied and the last adhesive dressing is applied, The orders (time 1) and (time 2) will be issued by the surgeon. In this way, two different times for surgery will be measured.;Time of incision. Timepoint: During surgery. Method of measurement: By using an electronic timer, the incision time is measured so that when the skin incision starts, the surgeon gives the order (start) and the researcher starts measuring the time, and when the rectus sheath incision starts, the surgeon will give the order (end). In this way, the incision time will be measured.;Time of enucleation. Timepoint: During surgery. Method of measurement: Using an electronic timer, the enucleation time is measured so that when the surgeon's hand enters the bladder for enucleation, the surgeon gives the order (start) and the researcher starts measuring the time, and when all the desired parts of the prostate come out. The surgeon will give the order (end). In this way, the enucleation time will be measured.;After surgery pain. Timepoint: Immediately after surgery, 12 hours after surgery and 24 hours after surgery. Method of measurement: Visual analogue scale will be used to evaluate postoperative pain. The scale consists of a 10 cm line with descriptive words at both ends. In most pain studies, the range is written from "no pain" to "severe pain" or "worst pain ever." In the current study, the phrases "no pain" to "the worst pain ever" will be used on both sides of the mentioned line. Patients estimate their pain level by placing a mark on the line. Then the distance from the "no pain" point is measured with a ruler. In order to validate the data obtained, a single ruler will be used throughout the data collection.;Aft | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMojtaba Moradzadeh
Hamedan University of Medical Sciences
Outcome results
None listed