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Mesh Versus Suture Repair for Umbilical Hernias (HUMP)

Primary Purpose

Umbilical Hernia

Status
Completed
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
primary suture closure
mesh enforced closure
Sponsored by
Ruth Kaufmann, MD
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Umbilical Hernia focused on measuring umbilical, hernia, mesh

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Primary umbilical hernia
  • Signed Informed consent

Exclusion Criteria:

  • Umbilical hernia ≥ 4 cm diameter
  • Recurrence
  • Midline laparotomy
  • Ascites/Cirrhosis
  • ASA score IV or above
  • Incarcerated hernia/emergency procedures

Sites / Locations

  • Studienzentrum der Deutschen Gesellschaft für Chirurgie
  • University of Witten/Herdecke
  • Multimedica
  • Erasmus University Medical Center
  • Onze Lieve Vrouwe Gasthuis
  • Wilhelmina Ziekenhuis
  • Reinier de Graaf Gasthuis
  • Havenziekenhuis
  • Ikazia
  • Maasstad Ziekenhuis
  • Máxima Medisch Centrum
  • Isala

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

primary suture

mesh enforced closure

Arm Description

Outcomes

Primary Outcome Measures

hernia recurrence rate

Secondary Outcome Measures

Post-operative morbidity and complications

Full Information

First Posted
November 9, 2008
Last Updated
February 22, 2018
Sponsor
Ruth Kaufmann, MD
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1. Study Identification

Unique Protocol Identification Number
NCT00789230
Brief Title
Mesh Versus Suture Repair for Umbilical Hernias
Acronym
HUMP
Official Title
Mesh Versus Suture Repair for Umbilical Hernias: a Double Blinded, Randomised Controlled Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
February 2018
Overall Recruitment Status
Completed
Study Start Date
January 2006 (undefined)
Primary Completion Date
April 2015 (Actual)
Study Completion Date
August 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Ruth Kaufmann, MD

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of the present study is to investigate whether or not the use of mesh is indicated in the repair of all size umbilical hernias as to reduce the rate of recurrence. This method is regularly used in umbilical hernia reconstruction although most surgeons repair small hernias using suture repair (fascia adaptation). Especially risk factors for hernia recurrence such as hernia size and BMI > 30 kg/m2 need to be evaluated and correlated to the method of hernia repair.
Detailed Description
Purpose The purpose of the present study is to investigate whether or not the use of mesh is indicated in the repair of all size umbilical hernias as to reduce the rate of recurrence. This method is regularly used in umbilical hernia reconstruction although most surgeons repair small hernias using suture repair (fascia adaptation). Especially risk factors for hernia recurrence such as hernia size and BMI > 30 kg/m2 need to be evaluated and correlated to the method of hernia repair. Study design Randomised controlled, double blinded, multi-centre trial. 300 consecutive patients with an umbilical hernia will be included in the study. Patients will be randomised in one of two groups of 150 patients each. Group 1 will include patients that will undergo primary (suture) repair; group 2 umbilical hernias will be repaired using a pre-peritoneal, flat polypropylene mesh in a tension free fashion. Stratification will be utilized for the size of the hernia (1-2 cm or ≥2-4 cm) and the participating centre. Patients will visit the outpatient clinic after 2-3 weeks and after 3, 12 and 24 months. The cumulative hernia recurrence rate during the 2-years follow-up period will be the primary outcome of the study. Complications, pain and QOL are secondary endpoints. Statistical analysis All analyses will be performed according to the intention to treat principle and as specified in the protocol. Financial support None.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Umbilical Hernia
Keywords
umbilical, hernia, mesh

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Suture versus mesh repair in umbilical hernia patients
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
300 (Actual)

8. Arms, Groups, and Interventions

Arm Title
primary suture
Arm Type
Active Comparator
Arm Title
mesh enforced closure
Arm Type
Active Comparator
Intervention Type
Procedure
Intervention Name(s)
primary suture closure
Intervention Description
primary suture closure of hernia
Intervention Type
Device
Intervention Name(s)
mesh enforced closure
Intervention Description
mesh enforced closure of hernia
Primary Outcome Measure Information:
Title
hernia recurrence rate
Time Frame
24 months
Secondary Outcome Measure Information:
Title
Post-operative morbidity and complications
Time Frame
3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Primary umbilical hernia Signed Informed consent Exclusion Criteria: Umbilical hernia ≥ 4 cm diameter Recurrence Midline laparotomy Ascites/Cirrhosis ASA score IV or above Incarcerated hernia/emergency procedures
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
J. Jeekel, MD, PhD
Organizational Affiliation
Erasmus Medical Center
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
J.F. Lange, MD, PhD
Organizational Affiliation
Erasmus Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Studienzentrum der Deutschen Gesellschaft für Chirurgie
City
Heidelberg
Country
Germany
Facility Name
University of Witten/Herdecke
City
Witten
Country
Germany
Facility Name
Multimedica
City
Milano
Country
Italy
Facility Name
Erasmus University Medical Center
City
Rotterdam
State/Province
Zuid Holland
ZIP/Postal Code
3015CN
Country
Netherlands
Facility Name
Onze Lieve Vrouwe Gasthuis
City
Amsterdam
Country
Netherlands
Facility Name
Wilhelmina Ziekenhuis
City
Assen
Country
Netherlands
Facility Name
Reinier de Graaf Gasthuis
City
Delft
Country
Netherlands
Facility Name
Havenziekenhuis
City
Rotterdam
Country
Netherlands
Facility Name
Ikazia
City
Rotterdam
Country
Netherlands
Facility Name
Maasstad Ziekenhuis
City
Rotterdam
Country
Netherlands
Facility Name
Máxima Medisch Centrum
City
Veldhoven
Country
Netherlands
Facility Name
Isala
City
Zwolle
Country
Netherlands

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
29459021
Citation
Kaufmann R, Halm JA, Eker HH, Klitsie PJ, Nieuwenhuizen J, van Geldere D, Simons MP, van der Harst E, van 't Riet M, van der Holt B, Kleinrensink GJ, Jeekel J, Lange JF. Mesh versus suture repair of umbilical hernia in adults: a randomised, double-blind, controlled, multicentre trial. Lancet. 2018 Mar 3;391(10123):860-869. doi: 10.1016/S0140-6736(18)30298-8. Epub 2018 Feb 17.
Results Reference
derived

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Mesh Versus Suture Repair for Umbilical Hernias

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