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Clinical Trials/NCT01348477
NCT01348477UnknownNot Applicable

Comparison Between Elliptical Domed Mesh Technique and Lichtenstein Technique, to Reduce Postoperative Pain in Open Inguinal Hernia Repair

Instituto Mexicano del Seguro Social1 site in 1 country168 target enrollmentStarted: October 2010Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Enrollment
168
Locations
1
Primary Endpoint
pain one month after surgery

Study Overview

Brief Summary

The investigators describe a new surgical technique for inguinal hernia open repair, which will be compared with the Lichtenstein technique. The investigators seek to find the difference between the two techniques in postoperative pain.

Detailed Description

The investigators randomly assigned 168 adult patients with uncomplicated primary inguinal hernia to two treatment groups:

Group A: 84 patients treated with the new technique Group B: 84 patients treated with the technique of Lichtenstein (gold standard) The investigators reviewed the patients operated on one week, one month, three months and six months after surgery. The investigators evaluated the presence of moderate to severe pain in each technique, as well as the intensity of pain, measured by visual analogue scale.

The investigators also determined the presence of inguinal dysesthesias in each technique, measured by dermatome mapping.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Double (Participant, Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • adult patients diagnosed with uncomplicated primary inguinal hernia
  • mentally healthy patients
  • patients without preoperative groin pain
  • patients eligible for outpatient surgery

Exclusion Criteria

  • patients with different surgical diagnosis

Outcomes

Primary Outcomes

pain one month after surgery

Time Frame: one month

Pain will be measured by the Visual Analogue Scale, from zero to ten. Measurements will be made per month, three months and six months after surgery. With these data we will built two survival curves (one for each group)with the proportions of patients still have pain in every time frame. We will compare the two curves with logrank statistic test.

pain three months after surgery

Time Frame: three months

Pain will be measured by the Visual Analogue Scale, from zero to ten. Measurements will be made per month, three months and six months after surgery. With these data we will built two survival curves (one for each group)with the proportions of patients still have pain in every time frame. We will compare the two curves with logrank statistic test.

pain six months after surgery

Time Frame: six months

Pain will be measured by the Visual Analogue Scale, from zero to ten. Measurements will be made per month, three months and six months after surgery. With these data we will built two survival curves (one for each group)with the proportions of patients still have pain in every time frame. We will compare the two curves with logrank statistic test.

Secondary Outcomes

  • dysesthesia one month after surgery(one month)
  • dysesthesia three months after surgery(three months)
  • dysesthesia six months after surgery(six months)

Investigators

Sponsor Class
Other Gov

Study Sites (1)

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