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Randomized Controlled Study Comparing Three Different Techniques for Open Hernia Repair

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Karolinska Institute

Status

Completed

Conditions

Inguinal Hernia

Treatments

Procedure: Hernia repair

Study type

Interventional

Funder types

Other

Identifiers

NCT01699971
2006/672-31/4

Details and patient eligibility

About

The primary aim is to evaluate if PSH and/or ultrapro mesch reduces chronic groin pain postoperatively compared to lichtenstein mesh. The second aim is to evaluate quality of life, recovery from surgery and frequency of recurrencies in the three groups

Enrollment

160 patients

Sex

Male

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 18-75 years
  • unilateral primary hernia
  • open surgery

Exclusion criteria

  • Recurrent Hernia
  • Bilateral Hernia
  • laparoscopic surgery
  • Female

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

160 participants in 1 patient group

Lichtenstein
Active Comparator group
Description:
Hernia repair with lichtenstein propylene mesh
Treatment:
Procedure: Hernia repair
Procedure: Hernia repair
Procedure: Hernia repair

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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