NCT06209450

Brief Summary

Comparison beta sutured and suturless mesh fixation for ventral hernia regarding recurrence rates and complications rate

Trial Health

35
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
1

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Mar 2024

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

January 5, 2024

Completed
12 days until next milestone

First Posted

Study publicly available on registry

January 17, 2024

Completed
1 month until next milestone

Study Start

First participant enrolled

March 1, 2024

Completed
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 1, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

March 1, 2025

Completed
Last Updated

January 17, 2024

Status Verified

January 1, 2024

Enrollment Period

1 year

First QC Date

January 5, 2024

Last Update Submit

January 5, 2024

Conditions

Ventral Hernia

Outcome Measures

Primary Outcomes (1)

  • Complications

    Intraoperative and post operative complications occur due to technique used in study

    One year after surgery

Study Arms (1)

Ventral hernia repair

EXPERIMENTAL
Procedure: Ventral hernia repair with mesh fixation

Interventions

Ventral hernia repair with mesh fixationPROCEDURE

Sutured versus suturless mesh fixation

Ventral hernia repair

Eligibility Criteria

Age18 Years - 60 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • ventral hernia
  • both sexes

You may not qualify if:

  • obstructed or complicated ventral hernia
  • incisional hernia
  • recurrent hernia
  • multiple ventral hernia
  • large hernia more than 5 cm

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Hernia, Ventral

Condition Hierarchy (Ancestors)

Hernia, AbdominalHerniaPathological Conditions, AnatomicalPathological Conditions, Signs and Symptoms

Central Study Contacts

Khaled Muhammad Mahmoud

CONTACT

01069094017Khaledgad19844@gmail.com

Moray Muhammad Morsy, Prof

CONTACT

01093688097m.morsy@aun.edu.eg

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assuit

Study Record Dates

First Submitted

January 5, 2024

First Posted

January 17, 2024

Study Start

March 1, 2024

Primary Completion

March 1, 2025

Study Completion

March 1, 2025

Last Updated

January 17, 2024

Record last verified: 2024-01