NCT06757998

Brief Summary

To compare between the outcome of on-lay and pre-peritoneal techniques of hernioplasty in incisional lumbar hernia repair.

Trial Health

65
Monitor

Trial Health Score

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

Enrollment
30

participants targeted

Target at below P25 for all trials

Timeline
7mo left

Started Dec 2024

Status
not yet recruiting

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

Study Progress68%
Dec 2024Dec 2026

First Submitted

Initial submission to the registry

December 27, 2024

Completed
2 days until next milestone

Study Start

First participant enrolled

December 29, 2024

Completed
5 days until next milestone

First Posted

Study publicly available on registry

January 3, 2025

Completed
1.9 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 30, 2026

Expected
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

December 30, 2026

Last Updated

January 3, 2025

Status Verified

December 1, 2024

Enrollment Period

1.9 years

First QC Date

December 27, 2024

Last Update Submit

December 27, 2024

Conditions

Lumbar Hernia

Outcome Measures

Primary Outcomes (1)

  • Short term complications (Recurrence, Postoperative Seroma and skin infection.)

    Two months

Interventions

MeshPROCEDURE

Compare between On-lay versus pre-peritoneal hernioplasty in incisional lumbar herni

Eligibility Criteria

Age18 Years - 60 Years
Sexall
Age GroupsAdult (18-64)
Sampling MethodNon-Probability Sample
Study Population

• Conventional Sample size of about 30 Cases about 15 cases of each group

You may qualify if:

  • Incisional lumbar hernia
  • Recurrent lumbar hernia
  • Age more than 16 years old

You may not qualify if:

  • Complicated lumbar hernia (irreducible, obstructed, strangulated hernia)
  • Denovo lumbar hernia

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Hernia

Interventions

Melanocyte-Stimulating Hormones

Condition Hierarchy (Ancestors)

Pathological Conditions, AnatomicalPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

MelanocortinsPro-OpiomelanocortinHypothalamic HormonesPeptide HormonesHormonesHormones, Hormone Substitutes, and Hormone AntagonistsPituitary Hormones, AnteriorPituitary HormonesNeuropeptidesPeptidesAmino Acids, Peptides, and ProteinsNerve Tissue ProteinsProteins

Central Study Contacts

Ali Fathy

CONTACT

01030501745alisfathy111@gmail.com

Ibrahim Mostafa

CONTACT

01140024448dr_ibrahim.alouny@yahoo.com

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
AFAli

Study Record Dates

First Submitted

December 27, 2024

First Posted

January 3, 2025

Study Start

December 29, 2024

Primary Completion (Estimated)

November 30, 2026

Study Completion (Estimated)

December 30, 2026

Last Updated

January 3, 2025

Record last verified: 2024-12