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Compares treatment options for Inguinal Hernia Unilateral
Official title Desarda Tissue Technique vs Lichtenstein Technique for Primary Inguinal Hernia Repair
ClinicalTrials.gov ID: NCT06650878
What this study is testing
- What it's testing
- This study aims to evaluate whether a surgical technique (Desarda) is superior to the commonly used surgical technique (Lichtenstein) in inguinal hernia repair concerning the occurrence of postoperative complications. The Lichtenstein technique involves the use of a mesh, while the Desarda technique does not.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 and older
You may be able to join if
- Diagnosed with primary inguinal hernia.
- Body mass index below 31
- Indication for inguinal hernia repair via anterior approach, either as outpatient surgery (CMA) or elective admission.
- Legal capacity to provide informed consent.
You likely can't join if
- Patients with a weak, thin, or divided external oblique aponeurosis.
- Participants diagnosed with any of the following conditions:
- Ongoing oncological disease
- Cirrhotic patients classified as Child B or higher
- Women who have previously undergone a cesarean section
- Cognitive or affective conditions that limit the ability to cooperate with the study procedures
The study team makes the final eligibility decision.
Where it's taking place
- Sant Pere de Ribes, Barcelona, Spain
Compensation & support
Compensation mentioned.
ClinicalTrials.gov doesn't provide a reliable structured field for payment or travel support - confirm details with the study team.
Questions & answers
Do participants get paid in this trial?
This study's listing includes signals that participants may be compensated or receive a stipend. Amounts vary and are set by the study team - confirm the details with them.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years and older. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Sant Pere de Ribes, Barcelona, Spain. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.