Sexual Dysfunction After Renal Transplantation
Sponsor
Xijing Hospital (Other)
Overall Status
Recruiting
CT.gov ID
NCT05856929
Collaborator
(none)
500
2
20
250
12.5
Study Details
Study Description
Brief Summary
A questionnaire will be send to kidney transplant recipients to investigate characteristics of them and their sexual function, all participants in the survey are anonymous and voluntary, then analyse these characteristics.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Study Design
Study Type:
Observational
Anticipated Enrollment
:
500 participants
Observational Model:
Other
Time Perspective:
Cross-Sectional
Official Title:
Sexual Function and Reproductive Function of Kidney Transplant Recipients
Actual Study Start Date
:
Oct 1, 2022
Anticipated Primary Completion Date
:
Jan 1, 2024
Anticipated Study Completion Date
:
Jun 1, 2024
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Renal transplant group
|
Other: no Intervention
no intervention
|
Outcome Measures
Primary Outcome Measures
- the number of participants is up to 500 [2024.06]
Eligibility Criteria
Criteria
Ages Eligible for Study:
18 Years
to 70 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
- patients who have undergone kidney transplantation for more than six months
Exclusion Criteria:
- having no sexual partner, being under 18 or over 70 years of age, exhibiting abnormal mental behavior, having poor understanding and communication ability, having low intelligence, or having a congenital sexual disorder
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Xijing Hospital | Xi'an | Shaanxi | China | 710032 |
| 2 | Department of Urology | Xi'an | China | 710032 |
Sponsors and Collaborators
- Xijing Hospital
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.Responsible Party:
Xijing Hospital
ClinicalTrials.gov Identifier:
NCT05856929
Other Study ID Numbers:
- KY20222236-C-1
First Posted:
May 12, 2023
Last Update Posted:
May 12, 2023
Last Verified:
Sep 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Product Manufactured in and Exported from the U.S.:
No