Mesh Fixation
ProcedureMesh fixation during Lichtenstein inguinal hernia repair.
NCT Number: NCT07210424
We are going to see the outcome measures for patient and compare them across two groups, those who are undergoing mesh fixation for inguinal hernia by sutures, and those who are fixated by skin staples.
Trial opening soon.
Get Notified18 year–65 year
All sexes
Observational
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Mesh fixation during Lichtenstein inguinal hernia repair.
Time frame: At 3, 7, 14 and 30 post op day
Pain scores at 3, 7, 14 and 30 days using a Visual Analogue Pain Scale with values ranging between 0 to 10, 0 meaning no pain and 10 being the highest level of pain.
King Edward Medical University
Other
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT07680777
Hernia, Hernia, Abdominal
Edmonton, Alberta, Canada
View Trial DetailsNCT07267494
Diastasis Recti, Hernia
Sacramento, California, United States
View Trial DetailsNCT07319754
Hernia, Hernia, Abdominal
Adana, Turkey (Türkiye)
View Trial DetailsNCT06975826
Hernia, Hernia, Abdominal
View Trial Details