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CompletedNCT01105039Updated Apr 18, 2011

Detailed Pain Pattern After Laparoscopic Inguinal Hernia Repair

An observational study in Inguinal Hernia and Femoral Hernia, sponsored by Zealand University Hospital. Completed at 1 site in Denmark. Open to male participants aged 18 Years to 69 Years. Per ClinicalTrials.gov, last updated 2011-04-18.

Sponsored by Zealand University Hospital · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
50
Ages
18 Years to 69 Years
Sex
Male
01

Study summary

Pain after laparoscopic groin hernia repair consist of different pain components (overall pain, shoulder pain, incisional pain and visceral pain). Thus it is important to find out which of these pain components that is most severe, so intervention can be targeted.

Read the detailed description

Details about the components of early pain after laparoscopic groin hernia repair are lacking. A description of each component (overall pain, shoulder pain,incisional pain and visceral pain) is needed, so intervention against the different pain components can be targeted.

Patients fill out questionnaires about pain before operation and day 0-3 after operation.

02

Conditions studied

  • Inguinal Hernia
  • Femoral Hernia

Keywords

  • Pain pattern
  • overall pain
  • incisional pain
  • shoulder pain
  • visceral pain
03

In context

Hernia

1,096 studies on the registry are indexed under Hernia; 132 are open to participants now.

This study's enrollment of 50 is below the median of 120 across 327 observational studies indexed under Hernia.

Browse Hernia studies →

Lead sponsor

Zealand University Hospital is the lead sponsor of 234 studies on the registry; 51 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 69 Years
Sexes eligible
Male
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

Patients are consecutively included in this study. They are all undergoing elective laparoscopic groin hernia repair.

Inclusion criteria

  • men
  • 18-69 years
  • uni- or bilateral hernia
  • ASA I-II
  • Danish speaking

Exclusion criteria

Exclusion Criteria:

  • bad compliance
  • acute operation
  • daily intake of opioids
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
50 participants (actual)

Groups and cohorts

  • lap. hernia repair

    undergoing laparoscopic groin hernia repair

06

What researchers measure

Primary outcomes

  1. Overall pain during coughing (visual analog scale)

    Time frame: 3 days

Secondary outcomes

  1. shoulder pain during coughing (visual analog scale and verbal rating scale)

    Time frame: 3 days

  2. incisional pain during coughing (visual analog scale and verbal rating scale)

    Time frame: 3 days

  3. visceral pain during coughing (visual analog scale and verbal rating scale)

    Time frame: 3 days

07

Study locations

1 site
  • University Hospital Koge
    Koge, Sealand 4600, Denmark
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 18, 2011, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01105039
Lead sponsor
Zealand University Hospital
First posted
Apr 16, 2010
Start date
Nov 2009
Primary completion
Aug 2010
Completion
Sep 2010
Last update
Apr 18, 2011

Study contacts

Mette A Tolver, M.D.
principal investigator · Koge Hospital

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Feb 2011. You cannot join it, but the record below documents what was studied.

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