Conversion of Evidence and Applied Research on Intermittent Catheterization After Radical Hysterectomy

West China Second University Hospital

Status

Enrolling

Conditions

Intermittent Catheterization

Conversion of Evidence

Treatments

Behavioral: intermittent catheterization protocol based on the best evidence

Study type

Interventional

Funder types

Other

Identifiers

NCT06529107

2023203

Details and patient eligibility

About

In this study, the investigators summarize the existing best evidence of intermittent catheterization in patients after radical cervical cancer surgery from the perspective of clinical translation of evidence through systematic search, evaluation and evidence integration, construct a nursing protocol of intermittent catheterization for patients after radical cervical cancer surgery based on the best evidence combined with the clinical context, and explore the clinical application effect of the above nursing protocol. It will provide a reference basis for the development of the standardization and management of intermittent catheterization for postoperative patients with cervical cancer in China, as well as the development of guidelines for intermittent catheterization after radical cervical cancer surgery.

Enrollment

70 estimated patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Age ≧ 18 years old
Radical cervical cancer surgery and intermittent catheterization were performed at the Institute's hospital
Patients or their family members can operate a smartphone
No cognitive or psychiatric disorders, and can communicate effectively

Exclusion criteria

People with serious heart, brain, lung and other important organ diseases
People with water, electrolyte, acid-base balance disorders at the beginning of intermittent catheterization
People with previous serious renal diseases, bladder and urethra surgery
People with urinary tract infections
People who did not complete all interventions or data collection
People who voluntarily withdrew from the study or died during the study period;
Refuse to participate in this study