Skip to content

Randomized, open-label, prospective, and parallel-group comparison study on the effect of discharge instruction with Leaflet for the patients who have received renal cryotherapy.

Randomized, open-label, prospective, and parallel-group comparison study on the effect of discharge instruction with Leaflet for the patients who have received renal cryotherapy. - The effect of discharge instruction with Leaflet for the patients who have received renal cryotherapy.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000022068
Enrollment
30
Registered
2016-07-01
Start date
2016-07-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

renal cell carcinoma

Interventions

Leaflet describing the daily care and symptoms after the cryoablation. No using leaflet.

Sponsors

Okayama University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria: The subjects must meet all of the criteria as follows: 1) Patients who have been diagnosed with renal cell carcinoma before the cryoablation 2) Patients who have undergone cryoablation at our hospital 3) Patient age is greater than or equal to 20 years of age at the time of obtaining informed consent 4) Patients who obtained the document consent from an individual's discretion after receiving the sufficient explanation about participation in the study and understanding it adequately 5) Patients who are hospitalized 6) Patients who can response to the phone one week later from hospital discharge

Exclusion criteria

Exclusion criteria: Exclusion criteria: Patients who conflict with one of the followings are excluded from this study: 1)Patients who have a hearing disorder and are difficult to answer the phone 2)Patients who are cognitive impairment and difficult to answer the phone 3)Patients who have suffered from a mental illness and are difficult to answer the phone 4)Patients who cannot make decisions for consent about the research by himself or herself 5)Patients who have been determined to be inappropriate for participating the study by doctors or researchers

Design outcomes

Primary

MeasureTime frame
The ratio of patients who have experienced pains, fevers, or anxiety within one week after discharge.

Secondary

MeasureTime frame
1. The ratio of patients who have experienced pains, fevers, or numbness within one week after discharge. 2. The ratio of patients who have tried to improve daily life styles (e.g., taking antifebriles, keeping themselves clean, and striving to intake water). 3. Subjective evaluations of the Leaflet by patients.

Countries

Japan

Contacts

Public ContactYuriko Iwasa

Okayama University Hospital nursing department

nj8190_1@yahoo.co.jp086-223-7151

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026