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Development and Application Research of Planar Drainage Bag Clamp in Early Mobilization after Gynecological Oncology Surgery

Development and Application Research of Planar Drainage Bag Clamp in Early Mobilization after Gynecological Oncology Surgery

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500104388
Enrollment
Unknown
Registered
2025-06-16
Start date
2025-06-16
Completion date
Unknown
Last updated
2025-06-24

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

Conditions

Gynecological Oncology

Interventions

Control group:Before surgery, patients will receive education through the cloud follow-up system and WeChat public account, distributing health education materials and videos. The content includes inf
postoperative dietary care
preventive measures for postoperative complications
the purpose of drainage tube placement, precautions during the period with the tube, and how to deal with emergencies. After surgery, the drainage tube will be securely fixed using the high platform m
Experimental group:On the basis of routine nursing care, the planar drainage bag clamp device will be provided. A member of the research team will attach the drainage bag to the main body of the devic

Sponsors

Women's Hospital School of Medicine Zhejiang University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Age >=18 years; 2. Patients diagnosed with gynecological tumors and scheduled for surgical treatment; 3. Postoperative retention of abdominal drainage tubes and/or other drainage tubes; 4. Barthel Index (BI) score >=60 points; 5. Normal mental status of the patient, with no history of mental illness; 6. Patient and family members agree to participate in this study; 7. No communication barriers.

Exclusion criteria

Exclusion criteria: 1. Patients with mental illness or a history of mental illness; 2. Patients who are deaf-mute or have communication barriers; 3. Patients who are blind or have severe visual impairments; 4. Patients who are pregnant; 5. Patients with severe dysfunction of vital organs such as the heart, brain, or kidneys; 6. Patients or their family members are unwilling to participate in this study.

Design outcomes

Primary

MeasureTime frame
Time to first ambulation;Daily walking distance during the period with the drainage tube;

Secondary

MeasureTime frame
State of anxiety;Traction pain during activities with drainage tubes in place;Time to first anal exhaust;Time to first defecation;Unplanned Extubation Rate;

Countries

China

Contacts

Public ContactJiaojiao Feng

Women's Hospital School of Medicine Zhejiang University

jj19871221@126.com+86 137 3552 5620

Outcome results

None listed

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