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Exploring risk factors affecting intraoperative safety profiles in high risk patients undergoing transurethral plasmakinetic resection of the prostate: a prospective clinical study based on endoscopic surgical monitor

Exploring risk factors affecting intraoperative safety profiles in high risk patients undergoing transurethral plasmakinetic resection of the prostate: a prospective clinical study based on endoscopic surgical monitor

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300070359
Enrollment
Unknown
Registered
2023-04-10
Start date
2023-04-15
Completion date
Unknown
Last updated
2024-10-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Benign prostatic hyperplasia

Interventions

Sponsors

Lanzhou University Second Hospital
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: 1.Suffer from benign prostatic hyperplasia (BPH) and meet the surgical indications of transurethral plasmakinetic resection of the prostate(PK-TURP)surgery (meet one or more of the following conditions) : (1)Maximum urinary flow rate = 8, lower urinary tract symptoms have significantly affected the quality of life, especially for those who have had ineffective drug treatment or refuse to receive drug treatment 2. Preoperative anesthesia grade ASA>= 3 3. The patient can understand and sign the informed consent form for surgery

Exclusion criteria

Exclusion criteria: 1.Patients with severe cardiovascular or cerebrovascular diseases, respiratory diseases, blood coagulation dysfunction, or liver or kidney dysfunction who can not tolerate surgery or anesthesia 2.Patients with neurogenic bladder, bladder neck contracture, bladder stone or bladder tumor 3.Patients with severe urinary tract infection before surgery 4.Collection of irrigation fluid leakage during the operation 5.Patients with mental disorders, or spinal or leg malformation or functional disorders can not maintain lithotomy position during the operation 6.Patients with severe urethral stricture can not be treated with surgery temporarily 7.Patients refuse to accept surgical treatment or participate in this study

Design outcomes

Primary

MeasureTime frame
Fluid absorption volume;Blood loss volume;

Secondary

MeasureTime frame
Risk factors for fluid absorption volume and blood loss volume;Immediate postoperative red blood cell count (RBC), hemoglobin concentration (HB), hematocrit (HCT), Na+ concentration, Cl- concentration, K+ concentration, Mg2+ concentration, Ca2+ concentration;Intraoperative and postoperative complications;Postoperative bladder irrigation time;Postoperative indwelling catheter time;Postoperative hospital stay time;

Countries

China

Contacts

Public ContactZhiping Wang

Lanzhou University Second Hospital

wangzplzu@163.com+86 13893131697

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026