Tokyo, Aug. 30 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000058610) titled 'A prospective, observational study on quality of life 6 months after treatment for chronic postoperative inguinal pain according to the Hernia-Related Quality-of-Life Survey' on Aug. 30.
Study Type:
Observational
Primary Sponsor:
Institute - Kobe city Medical Center General Hospital
Condition:
Condition - Patients with chronic postoperative inguinal pain
Classification by malignancy - Others
Genomic information - NO
Objective:
Narrative objectives1 - The aim of the present prospective cohort study is to evaluate quality of life 6 months after treatment for chronic postoperative inguinal pain according to the hernia-related quality-of-life survey.
Basic objectives2 - Efficacy
Eligibility:
Age-lower limit - Not applicable
Age-upper limit - Not applicable
Gender - Male and Female
Key inclusion criteria - 1) Patients who want to be treated for CPIP
2) Patients who intend to participate the present study
Key exclusion criteria - N/A
Target Size - 40
Recruitment Status:
Recruitment status - Preinitiation
Date of protocol fixation - 2025 Year 07 Month 28 Day
Anticipated trial start date - 2025 Year 08 Month 30 Day
Last follow-up date - 2029 Year 03 Month 31 Day
To know more, visit https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000067017
Disclaimer: Curated by HT Syndication.
