Tension-free Repair of Inguinal Hernia With "Undissociate Spermatic Cord"
The First Affiliated Hospital of Harbin Medical Uniersity
1 other identifier
observational
134
0 countries
N/A
Brief Summary
The theory of "undissected Spermatic cord (US)" only transected the hernia ring ends in the abdominal cavity, the hernia ring, hernia sac and spermatic cord will not be dissected. Its significance lies in that inguinal hernia repair can get rid of the "entanglement" of hernia sac and spermatic cord and fundamentally change the treatment mode of hernia ring and hernia sac.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Mar 2014
Longer than P75 for all trials
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
March 1, 2014
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 1, 2019
CompletedStudy Completion
Last participant's last visit for all outcomes
March 1, 2019
CompletedFirst Submitted
Initial submission to the registry
January 21, 2022
CompletedFirst Posted
Study publicly available on registry
February 21, 2022
CompletedFebruary 21, 2022
February 1, 2022
5 years
January 21, 2022
February 9, 2022
Conditions
Keywords
Outcome Measures
Primary Outcomes (4)
surgery time
the operation time
0-120minutes
Bleeding
Blood loss
surgery
hospital stay
the hospitalization time
1-30days
Does it recur
Does it recur
18-63months
Study Arms (2)
experimental group
Tension-free repair of inguinal hernia with "Undissociate Spermatic cord"
control group
Tension-free repair of inguinal hernia with traditional method
Interventions
patient undergoing Tension-free repair of inguinal hernia with "Undissociate Spermatic cord"
Eligibility Criteria
inguinal hernia patients
You may qualify if:
- Inguinal hernia patients who can tolerate surgery
You may not qualify if:
- Patients who cannot tolerate surgery
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Deputy Chief Physician
Study Record Dates
First Submitted
January 21, 2022
First Posted
February 21, 2022
Study Start
March 1, 2014
Primary Completion
March 1, 2019
Study Completion
March 1, 2019
Last Updated
February 21, 2022
Record last verified: 2022-02
Data Sharing
- IPD Sharing
- Will not share