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Clinical effect evaluation of a new continuous bladder flushing and drainage device in nursing continuous bladder flushing after TURP

Clinical evaluation of a new continuous bladder flushing drainage device for continuous bladder flushing care after TURP: a single-center randomized controlled study

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100052886
Enrollment
Unknown
Registered
2021-11-06
Start date
2022-01-01
Completion date
Unknown
Last updated
2022-08-23

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

Conditions

Nursing after resection of prostate

Interventions

Experimental group:The new continuous drainage flask was used for drainage
Control group:Drainage using a chest drainage bottle

Sponsors

Peking University Shenzhen Hospital
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Aged >= 18 years; 2. Patients with prostatic hyperplasia who plan to undergo electroprostatectomy; 3. Patients who have the ability to sign informed consent and agree to participate in the study (informed consent must be approved by an independent ethics committee and informed consent must be obtained prior to the commencement of any study related process); 4. Participants can cooperate to complete the operation.

Exclusion criteria

Exclusion criteria: 1. Patients with previous bladder or prostate surgery; 2. Patients with coagulation dysfunction or blood diseases before surgery; 3. Severe insufficiency of heart, brain, liver, kidney and other organs; 4. Patients with diseases of immune system and mental system.

Design outcomes

Primary

MeasureTime frame
Total duration continuous bladder flushing care operation;

Secondary

MeasureTime frame
Degree of bladder spasm;Urinary tract blockages;Ongoing bladder irrigation costs;

Countries

China

Contacts

Public ContactZhao Zhengping

Peking University Shenzhen Hospital

474008399@qq.com+86 13923455809

Outcome results

None listed

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