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The Effect of Showering Within 48–72 Hours After Percutaneous Kyphoplasty on Incision Infection, Pain, Comfort, and Patient Satisfaction: A Randomized Controlled Trial

The Effect of Showering Within 48–72 Hours After Percutaneous Kyphoplasty on Incision Infection, Pain, Comfort, and Patient Satisfaction: A Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600128999
Enrollment
Unknown
Registered
2026-07-29
Start date
2026-09-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

osteoporotic vertebral compression fractures, OVCF

Interventions

Delayed showering group (control group):Routine postoperative incision care
Early showering group (experimental group):Early showering within 48–72 hours after surgery

Sponsors

The Second Affiliated Hospital of Wenzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Age =60 years. 2.Patients with osteoporotic vertebral compression fracture requiring single-level percutaneous kyphoplasty (PKP). 3.The participant or legally authorized representative understands the purpose and procedures of the trial and voluntarily signs the informed consent form. 4.Cardiopulmonary, hepatic, and renal functions are sufficient to tolerate surgery. 5.Patients without diabetes mellitus, or patients with diabetes mellitus whose blood glucose is well controlled. The preoperative glycemic control targets are as follows: preprandial blood glucose =7.8 mmol/L, postprandial blood glucose =10.0 mmol/L, and glycated hemoglobin (HbA1c) =7%. 6.Patients are able to shower postoperatively under the supervision of family members, or receive regular incision dressing changes at a medical institution. 7.Preoperative auxiliary examinations exclude the possibility of infection at other sites.

Exclusion criteria

Exclusion criteria: 1.Patients with osteoporotic vertebral compression fracture requiring multilevel percutaneous kyphoplasty (PKP). 2.The participant or legally authorized representative refuses to participate in the trial or fails to sign the preoperative informed consent form. 3.Patients with severe comorbid medical conditions who are unable to tolerate surgery. 4.Patients with diabetes mellitus that cannot be controlled within a short period. 5.Patients with infection at other sites, or abnormal infection-related indicators suggested by preoperative auxiliary examinations. 6.Patients who are unable to follow the postoperative incision care requirements for showering or incision dressing changes.

Design outcomes

Primary

MeasureTime frame
Incidence of postoperative superficial surgical site infection;

Secondary

MeasureTime frame
Postoperative patient comfort;Postoperative pain;Postoperative nursing costs;Postoperative patient satisfaction;

Countries

China

Contacts

Public ContactWu Yaosen

The Second Affiliated Hospital of Wenzhou Medical University

wys9453@126.com+86 577 8567 6096

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 10, 2026