Skip to content

Study on the timing of early catheter removal in patients with laparoscopic total hysterectomy

Study on the timing of early catheter removal in patients with laparoscopic total hysterectomy

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100051098
Enrollment
Unknown
Registered
2021-09-13
Start date
2021-10-01
Completion date
Unknown
Last updated
2022-05-16

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

Conditions

Uterine fibroids, adenomyosis, cervical intraepithelial lesions

Interventions

experimental group A:Catheterization was performed 10min after induction of general anesthesia, and the catheter was removed 3h after surgery
experimental group B:Catheterization was performed 10min after induction of general anesthesia, and the catheter was removed 3h after surgery
control group C:Catheterization was performed 10min after induction of general anesthesia, and the catheter was removed 6h after surgery

Sponsors

Women's Hospital School of Medicine Zhejiang Univercity
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Age: 18-60 years old; 2. Diagnosed as benign gynecological diseases, such as adenomyosis, uterine fibroids, cervical intraepithelial lesions, etc.; 3. Laparoscopic total hysterectomy with or without bilateral adnexectomy; 4. The anesthesia method is general anesthesia; 5. Have a good understanding ability, be willing to participate in this research, and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. Have a history of mental illness; 2. Combined with serious medical diseases, such as hypertension, diabetes, etc.; 3. Diagnosed as deep endometriosis; 4. The anesthesia method is epidural anesthesia; 5. Urinary tract infection and history of urinary system diseases before surgery; 6. The urinary system is injured during the operation, and the doctor will indwelling the urinary catheter for a long time after the operation; 7. The amount of intraoperative blood loss is >=500ml. Due to the need for observation and treatment of the disease, the patient will be transferred to the ICU after surgery; 8. Operation time > 2h; 9. Those who asked to withdraw in the middle of the study. Patients who are participating in other clinical studies. The investigators believe that other reasons are not suitable for clinical investigators.

Design outcomes

Primary

MeasureTime frame
First urination;Incidence of urinary retention;Incidence of urinary tract infection;

Secondary

MeasureTime frame
VAS when indwelling catheter;First time out of bed;Postoperative hospital stay;

Countries

China

Contacts

Public ContactZheng Xiaolong

Women's Hospital School of Medicine Zhejiang Univercity

zxlong@zju.edu.cn+86 18758189765

Outcome results

None listed

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