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GreenLight-XPS Laser Vapo-Enucleation versus GreenLight-XPS Laser Vaporization of the Prostate in the Treatment of Symptomatic Benign Prostatic Hyperplasia

GreenLight-XPS Laser Vapo-Enucleation versus GreenLight-XPS Laser Vaporization of the Prostate in the Treatment of Symptomatic Benign Prostatic Hyperplasia

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800015867
Enrollment
Unknown
Registered
2018-04-25
Start date
2018-04-10
Completion date
Unknown
Last updated
2018-04-30

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

Conditions

benign prostatic hyperplasia

Interventions

A:Photoselective Vapo-Enucleation of the Prostate
B:Photoselective Vaporization of the Prostate

Sponsors

Department of Urology, Southwest Hospital
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: Patients with benign prostatic hyperplasia combined with one of the following criteria can enter the study group: 1. Repeated urinary retention (at least one time after pulling out the catheter cannot be voided or two urinary retention); 2. Repeated hematuria, drug treatment is ineffective; 3. Recurrent urinary tract infection; 4. bladder calculi; 5. Secondary hydronephrosis (with or without renal impairment); 6. Combined with inguinal hernia, severe hemorrhoids or rectocele, and it is difficult to achieve therapeutic effect without removing urinary tract obstruction.

Exclusion criteria

Exclusion criteria: 1. Patients with progressive malignant tumor; 2. Diuretic muscle contractions are weak; 3. Combined with urethral stricture; 4. The combination of uncontrolled urinary tract infection causes bladder urethral dysfunction; 5. The combination of central or peripheral neuropathy causes bladder urethral dysfunction; 6. Patients with severe heart and lung disease cannot tolerate surgery and anesthesia; 7. Patients with coagulopathy; 8. Patients with mental disorders; 9. Patients who are considered unfit to participate in any other condition of the trial

Design outcomes

Primary

MeasureTime frame
Maximum flow rate (QMax);Inter-national Prostate Symptom Score;

Secondary

MeasureTime frame
post-void residual urine volume;prostate volume;prostate specific antigen;International Index of Erectile Function;Quality Of Life Score;operation duration;OABq-SF health;OABq-SF health;International Consulta-tion on Incontinence Questionnaire Short Form;Amount of bleeding in operation;

Countries

China

Contacts

Public ContactShen Wenhao

Department of Urology, Southwest Hospital

chongqingswh@aliyun.com+86 13983842766

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 11, 2026