Analysis of Risk Factors for Children With Heterochronous Indirect Hernia

NCT05092425 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 172

Last updated 2021-10-25

No results posted yet for this study

Summary

Laparoscopic contralateral patent processus vaginalis (CPPV) repair in infancy and childhood is still debatable, due to the high CPPV rate but low contralateral metachronous hernia (MCIH) rate. In order to found risk factors for MH, we conducted this prospective study.

This is an multi-center investigator-initiated observational prospective trial. After informed all the benefits and risks of repair CPPV simultaneously, those patients with unilateral inguinal hernia whose parents preferred not to repair CPPV simultaneously will be assigned in the study. All information about demographic data, hernia side, CPPV type and CPPV diameter will be recorded. The subjects will be followed up until MCIH developing or to 24 months postoperatively. Patients will be analyzed to identify the risk factors for MH.

Conditions

  • Inguinal Hernia, Direct
  • Child, Only
  • Laparoscopic Surgery

Interventions

OTHER

no intervention

no intervention

Sponsors & Collaborators

  • Children's Hospital of Hebei Province

    collaborator OTHER
  • Shengjing Hospital

    collaborator OTHER
  • Children's Hospital of Nanjing Medical University

    collaborator OTHER
  • Anhui Provincial Children's Hospital

    collaborator OTHER
  • Tianjin Children's Hospital

    collaborator OTHER
  • Shanxi Provincial Maternity and Children's Hospital

    collaborator OTHER
  • Tongji Hospital

    collaborator OTHER
  • Zunyi Medical College

    collaborator OTHER
  • Maternal and Child Health Hospital of Henan Province

    collaborator UNKNOWN
  • Shanghai Children's Hospital

    lead OTHER

Principal Investigators

  • Zhibao Lv, PhD · Shanghai Children's Hospital

Eligibility

Max Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-11-01
Primary Completion
2024-07-31
Completion
2024-07-31

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05092425 on ClinicalTrials.gov