benign prostatic hyperplasia
Conditions
Interventions
Experimental group:The rate of continuous bladder irrigation strategy+Routine guidance
Sponsors
The First Affiliated Hospital of Soochow University
Eligibility
Sex/Gender
Male
Inclusion criteria
Inclusion criteria: 1. It was diagnosed as prostatic hyperplasia by b-ultrasound, urodynamics, and serum prostatic specific antigen; 2. Preoperative coagulation was normal; 3. The surgical procedure was elective transurethral resection of the prostate; 4. Patients voluntarily participate in and sign informed consent.
Exclusion criteria
Exclusion criteria: 1. Patients with prostate cancer, neurogenic bladder, bladder neck sclerosis, and other urinary tract diseases; 2. Patients with other severe organic diseases; 3. Patients with a catheter indurated preoperative; 4. Patients with postoperative analgesia pump; 5. Patients who received a second operation due to secondary bleeding; 6. Patients with abnormal coagulation function postoperative; 7. Patients with postoperative cognitive impairment, language communication barriers or unwilling to cooperate.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Evaluation of bladder spasm; | — |
Secondary
| Measure | Time frame |
|---|---|
| Evaluation of blood clots blocking tubes;The amount of bladder irrigation fluid used;Total time for bladder flushing;Nursing satisfaction score; | — |
Countries
China
Contacts
Public ContactMa Zhengzheng
The First Affiliated Hospital of Soochow University
Outcome results
None listed